Canonical Allele Identifier: CA198901302

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114806920A>T , CM000671.2:g.114806920A>T	GRCh38
NC_000009.11:g.117569200A>T , CM000671.1:g.117569200A>T	GRCh37
NC_000009.10:g.116609021A>T	NCBI36
NG_011488.2:g.4209T>A