Canonical Allele Identifier: CA897878605

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119569567A>T , CM000665.2:g.119569567A>T	GRCh38
NC_000003.11:g.119288414A>T , CM000665.1:g.119288414A>T	GRCh37
NC_000003.10:g.120771104A>T	NCBI36