Canonical Allele Identifier: CA880851596

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.23966743C>G , CM000681.2:g.23966743C>G	GRCh38
NC_000019.9:g.24149545C>G , CM000681.1:g.24149545C>G	GRCh37
NC_000019.8:g.23941385C>G	NCBI36