Canonical Allele Identifier: CA858981139

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114806742A>T , CM000671.2:g.114806742A>T	GRCh38
NC_000009.11:g.117569022A>T , CM000671.1:g.117569022A>T	GRCh37
NC_000009.10:g.116608843A>T	NCBI36
NG_011488.2:g.4387T>A