Canonical Allele Identifier: CA188757925

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6365622T>C , CM000671.2:g.6365622T>C	GRCh38
NC_000009.11:g.6365622T>C , CM000671.1:g.6365622T>C	GRCh37
NC_000009.10:g.6355622T>C	NCBI36