Canonical Allele Identifier: CA671777989
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs1397962705
gnomAD v3: 11-112025319-C-T
gnomAD v4: 11-112025319-C-T
MyVariant Identifiers: chr11:g.112025319C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025319C>T , CM000673.2:g.112025319C>T GRCh38
NC_000011.9:g.111896043C>T , CM000673.1:g.111896043C>T GRCh37
NC_000011.8:g.111401253C>T NCBI36
NG_013342.1:g.5506C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-154C>T ENSP00000518862.1:n.-154C>T
ENST00000280346.10:c.-154C>T ENSP00000280346.6:n.-154C>T
NM_001931.4:c.-154C>T NP_001922.2:n.-154C>T
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