Canonical Allele Identifier: CA262978669

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65796245A>T , CM000676.2:g.65796245A>T	GRCh38
NC_000014.8:g.66262963A>T , CM000676.1:g.66262963A>T	GRCh37
NC_000014.7:g.65332716A>T	NCBI36