Canonical Allele Identifier: CA11462619
Gene: DGKG HGNC NCBI

Linked Data

dbSNP Id: rs7647305
gnomAD v2: 3-185834290-T-C
gnomAD v3: 3-186116501-T-C
gnomAD v4: 3-186116501-T-C
MyVariant Identifiers: chr3:g.185834290T>C (hg19) chr3:g.186116501T>C (hg38)
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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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