Canonical Allele Identifier: CA881650885

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33843009C>A , CM000681.2:g.33843009C>A	GRCh38
NC_000019.9:g.34333914C>A , CM000681.1:g.34333914C>A	GRCh37
NC_000019.8:g.39025754C>A	NCBI36