Canonical Allele Identifier: CA891214087

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172929171C>A , CM000663.2:g.172929171C>A	GRCh38
NC_000001.10:g.172898311C>A , CM000663.1:g.172898311C>A	GRCh37
NC_000001.9:g.171164934C>A	NCBI36