Canonical Allele Identifier: CA1462694263
Gene:

Linked Data

dbSNP Id: rs1756228414

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558187G>A , CM000666.2:g.62558187G>A GRCh38
NC_000004.11:g.63423905G>A , CM000666.1:g.63423905G>A GRCh37
NC_000004.10:g.63106500G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5657G>A