Canonical Allele Identifier: CA660496095

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117586341G>A , CM000672.2:g.117586341G>A	GRCh38
NC_000010.10:g.119345852G>A , CM000672.1:g.119345852G>A	GRCh37
NC_000010.9:g.119335842G>A	NCBI36