Canonical Allele Identifier: CA746612327

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.6645571G>T , CM000682.2:g.6645571G>T	GRCh38
NC_000020.10:g.6626218G>T , CM000682.1:g.6626218G>T	GRCh37
NC_000020.9:g.6574218G>T	NCBI36