Allele Registry

Canonical Allele Identifier: CA11462619

Gene: DGKG HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr3:g.186116501T>C

GRCh37 chr3:g.185834290T>C

Linked Data - Sequence & Population

gnomAD v2:

3:185834290 T / C

gnomAD v3:

3:186116501 T / C

gnomAD v4:

chr3-186116501-T-C

Joint Max Group AF 0.90580019 (EAS)

Genomes Max Group AF 0.90580019 (EAS)

Linked Data - NCBI & NCI

dbSNP:

7647305

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186116501T>C , CM000665.2:g.186116501T>C	GRCh38
NC_000003.11:g.185834290T>C , CM000665.1:g.185834290T>C	GRCh37
NC_000003.10:g.187316984T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447054.5:n.132-10559A>G

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