Canonical Allele Identifier: CA693150886

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88592239G>T , CM000674.2:g.88592239G>T	GRCh38
NC_000012.11:g.88986016G>T , CM000674.1:g.88986016G>T	GRCh37
NC_000012.10:g.87510147G>T	NCBI36