Canonical Allele Identifier: CA198901281

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114806739T>C , CM000671.2:g.114806739T>C	GRCh38
NC_000009.11:g.117569019T>C , CM000671.1:g.117569019T>C	GRCh37
NC_000009.10:g.116608840T>C	NCBI36
NG_011488.2:g.4390A>G