Canonical Allele Identifier: CA35069274
Gene:

Linked Data

dbSNP Id: rs565869657

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800698G>A , CM000663.2:g.192800698G>A GRCh38
NC_000001.10:g.192769828G>A , CM000663.1:g.192769828G>A GRCh37
NC_000001.9:g.191036451G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.128G>A