Canonical Allele Identifier: CA775173211

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76503318G>C , CM000679.2:g.76503318G>C	GRCh38
NC_000017.10:g.74499400G>C , CM000679.1:g.74499400G>C	GRCh37
NC_000017.9:g.72010995G>C	NCBI36
NG_032852.1:g.3110C>G , LRG_532:g.3110C>G