Canonical Allele Identifier: CA15808183
Gene:

Linked Data

dbSNP Id: rs12590640

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384931C>T , CM000676.2:g.36384931C>T GRCh38
NC_000014.8:g.36854136C>T , CM000676.1:g.36854136C>T GRCh37
NC_000014.7:g.35923887C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12228C>T XP_011535730.1:n.319-12228C>T
XR_943756.1:n.358+23835C>T