Canonical Allele Identifier: CA1500739169
Gene:

Linked Data

dbSNP Id: rs1727413876

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601442G>A , CM000666.2:g.144601442G>A GRCh38
NC_000004.11:g.145522594G>A , CM000666.1:g.145522594G>A GRCh37
NC_000004.10:g.145742044G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185464C>T ENSP00000497507.1:n.328-185464C>T