Canonical Allele Identifier: CA201726136

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137136549C>G , CM000671.2:g.137136549C>G	GRCh38
NC_000009.11:g.140031001C>G , CM000671.1:g.140031001C>G	GRCh37
NC_000009.10:g.139150822C>G	NCBI36
NG_011507.1:g.2393C>G