Canonical Allele Identifier: CA890355553

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.163063936A>G , CM000663.2:g.163063936A>G	GRCh38
NC_000001.10:g.163033726A>G , CM000663.1:g.163033726A>G	GRCh37
NC_000001.9:g.161300350A>G	NCBI36
NG_023312.1:g.331A>G