Canonical Allele Identifier: CA882121179

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39252541C>A , CM000681.2:g.39252541C>A	GRCh38
NC_000019.9:g.39743181C>A , CM000681.1:g.39743181C>A	GRCh37
NC_000019.8:g.44435021C>A	NCBI36
NG_055295.1:g.1316G>T