Canonical Allele Identifier: CA671777978
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs1291200891
gnomAD v4: 11-112025303-G-T
MyVariant Identifiers: chr11:g.112025303G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025303G>T , CM000673.2:g.112025303G>T GRCh38
NC_000011.9:g.111896027G>T , CM000673.1:g.111896027G>T GRCh37
NC_000011.8:g.111401237G>T NCBI36
NG_013342.1:g.5490G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-170G>T ENSP00000518862.1:n.-170G>T
ENST00000280346.10:c.-170G>T ENSP00000280346.6:n.-170G>T
NM_001931.4:c.-170G>T NP_001922.2:n.-170G>T
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