Canonical Allele Identifier: CA1500739094
Gene:

Linked Data

dbSNP Id: rs1727413295

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601409A>C , CM000666.2:g.144601409A>C GRCh38
NC_000004.11:g.145522561A>C , CM000666.1:g.145522561A>C GRCh37
NC_000004.10:g.145742011A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649263.1:c.328-185431T>G ENSP00000497507.1:n.328-185431T>G