Canonical Allele Identifier: CA198901300

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114806900A>G , CM000671.2:g.114806900A>G	GRCh38
NC_000009.11:g.117569180A>G , CM000671.1:g.117569180A>G	GRCh37
NC_000009.10:g.116609001A>G	NCBI36
NG_011488.2:g.4229T>C