Canonical Allele Identifier: CA693572559
Gene:

Linked Data

dbSNP Id: rs1436624637

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293260A>G , CM000674.2:g.93293260A>G GRCh38
NC_000012.11:g.93687036A>G , CM000674.1:g.93687036A>G GRCh37
NC_000012.10:g.92211167A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34767T>C