Canonical Allele Identifier: CA2000527676
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs1861925810
gnomAD v4: 11-112025329-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025329C>G , CM000673.2:g.112025329C>G GRCh38
NC_000011.9:g.111896053C>G , CM000673.1:g.111896053C>G GRCh37
NC_000011.8:g.111401263C>G NCBI36
NG_013342.1:g.5516C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-144C>G ENSP00000518862.1:n.-144C>G
ENST00000280346.10:c.-144C>G ENSP00000280346.6:n.-144C>G
NM_001931.4:c.-144C>G NP_001922.2:n.-144C>G
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