Canonical Allele Identifier: CA771902164

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39900944G>T , CM000679.2:g.39900944G>T	GRCh38
NC_000017.10:g.38057197G>T , CM000679.1:g.38057197G>T	GRCh37
NC_000017.9:g.35310723G>T	NCBI36