Canonical Allele Identifier: CA2615977020
Gene: DLAT HGNC NCBI

Linked Data

gnomAD v4: 11-112025332-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025332G>T , CM000673.2:g.112025332G>T GRCh38
NC_000011.9:g.111896056G>T , CM000673.1:g.111896056G>T GRCh37
NC_000011.8:g.111401266G>T NCBI36
NG_013342.1:g.5519G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-141G>T ENSP00000518862.1:n.-141G>T
ENST00000280346.10:c.-141G>T ENSP00000280346.6:n.-141G>T
NM_001931.4:c.-141G>T NP_001922.2:n.-141G>T
Search 100 bp 5'
Search 100 bp 3'