Canonical Allele Identifier: CA10633445
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs587665696
gnomAD v2: 11-111896107-G-C
gnomAD v3: 11-112025383-G-C
gnomAD v4: 11-112025383-G-C
MyVariant Identifiers: chr11:g.111896107G>C (hg19) chr11:g.112025383G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025383G>C , CM000673.2:g.112025383G>C GRCh38
NC_000011.9:g.111896107G>C , CM000673.1:g.111896107G>C GRCh37
NC_000011.8:g.111401317G>C NCBI36
NG_013342.1:g.5570G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-90G>C ENSP00000518862.1:n.-90G>C
ENST00000280346.10:c.-90G>C ENSP00000280346.6:n.-90G>C
NM_001931.4:c.-90G>C NP_001922.2:n.-90G>C
XM_011542647.1:c.-90G>C XP_011540949.1:n.-90G>C
XM_011542647.3:c.-90G>C XP_011540949.1:n.-90G>C
Search 100 bp 5'
Search 100 bp 3'