Canonical Allele Identifier: CA891771700

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17918213C>G , CM000663.2:g.17918213C>G	GRCh38
NC_000001.10:g.18244707C>G , CM000663.1:g.18244707C>G	GRCh37
NC_000001.9:g.18117294C>G	NCBI36