Canonical Allele Identifier: CA191256933

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22134163T>C , CM000671.2:g.22134163T>C	GRCh38
NC_000009.11:g.22134162T>C , CM000671.1:g.22134162T>C	GRCh37
NC_000009.10:g.22124162T>C	NCBI36