Canonical Allele Identifier: CA259369482
Gene:

Linked Data

dbSNP Id: rs371791556

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384902T>A , CM000676.2:g.36384902T>A GRCh38
NC_000014.8:g.36854107T>A , CM000676.1:g.36854107T>A GRCh37
NC_000014.7:g.35923858T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12257T>A XP_011535730.1:n.319-12257T>A
XR_943756.1:n.358+23806T>A