Canonical Allele Identifier: CA686513980

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.23270928A>T , CM000674.2:g.23270928A>T	GRCh38
NC_000012.11:g.23423862A>T , CM000674.1:g.23423862A>T	GRCh37
NC_000012.10:g.23315129A>T	NCBI36