Canonical Allele Identifier: CA837505141

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.3070425C>G , CM000669.2:g.3070425C>G	GRCh38
NC_000007.13:g.3110059C>G , CM000669.1:g.3110059C>G	GRCh37
NC_000007.12:g.3076585C>G	NCBI36