Hello,
I am a master student in genetics and using your website a lot to get
information regarding different genes. My question is I dont understand why,
when I look up a certain gene, I get several variation of it, which are
basicly all the same, and only differ in number of exons and coding exons as
it appears under description of the gene, but if I go to RefSeq accession,
under genomic alignments, I get a different no. of exons. For example I
could refer you to the gene HSKM-B. It has 2 variations, one is described
with 10 exons and non coding, the other with 8 exons and 7 coding. Under
genomic alignments there are 12 exons, all coding.

I would really appriciate you help.

Thank you in advance,

Danit.
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