Canonical Allele Identifier: CA692784881

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.84849902A>T , CM000674.2:g.84849902A>T	GRCh38
NC_000012.11:g.85243681A>T , CM000674.1:g.85243681A>T	GRCh37
NC_000012.10:g.83767812A>T	NCBI36