Canonical Allele Identifier: CA555410625
Gene:

Linked Data

dbSNP Id: rs1246040400

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601690G>T , CM000666.2:g.144601690G>T GRCh38
NC_000004.11:g.145522842G>T , CM000666.1:g.145522842G>T GRCh37
NC_000004.10:g.145742292G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185712C>A ENSP00000497507.1:n.328-185712C>A