Canonical Allele Identifier: CA198901275

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114806669G>A , CM000671.2:g.114806669G>A	GRCh38
NC_000009.11:g.117568949G>A , CM000671.1:g.117568949G>A	GRCh37
NC_000009.10:g.116608770G>A	NCBI36
NG_011488.2:g.4460C>T