Canonical Allele Identifier: CA10637612
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1210737
ClinVar RCV Id: RCV001581459
dbSNP Id: rs587688778
gnomAD v2: 11-111896040-G-A
gnomAD v3: 11-112025316-G-A
gnomAD v4: 11-112025316-G-A
MyVariant Identifiers: chr11:g.111896040G>A (hg19) chr11:g.112025316G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025316G>A , CM000673.2:g.112025316G>A GRCh38
NC_000011.9:g.111896040G>A , CM000673.1:g.111896040G>A GRCh37
NC_000011.8:g.111401250G>A NCBI36
NG_013342.1:g.5503G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-157G>A ENSP00000518862.1:n.-157G>A
ENST00000280346.10:c.-157G>A ENSP00000280346.6:n.-157G>A
NM_001931.4:c.-157G>A NP_001922.2:n.-157G>A
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