Canonical Allele Identifier: CA775346295

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78212770C>G , CM000679.2:g.78212770C>G	GRCh38
NC_000017.10:g.76208851C>G , CM000679.1:g.76208851C>G	GRCh37
NC_000017.9:g.73720446C>G	NCBI36
NG_029069.1:g.3575C>G