Canonical Allele Identifier: CA882121182

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39252548G>A , CM000681.2:g.39252548G>A	GRCh38
NC_000019.9:g.39743188G>A , CM000681.1:g.39743188G>A	GRCh37
NC_000019.8:g.44435028G>A	NCBI36
NG_055295.1:g.1309C>T