Canonical Allele Identifier: CA859651442

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121803541T>A , CM000671.2:g.121803541T>A	GRCh38
NC_000009.11:g.124565820T>A , CM000671.1:g.124565820T>A	GRCh37
NC_000009.10:g.123605641T>A	NCBI36