Canonical Allele Identifier: CA39184719

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.228862104G>A , CM000663.2:g.228862104G>A	GRCh38
NC_000001.10:g.228997851G>A , CM000663.1:g.228997851G>A	GRCh37
NC_000001.9:g.227064474G>A	NCBI36