Canonical Allele Identifier: CA2615977021
Gene: DLAT HGNC NCBI

Linked Data

gnomAD v4: 11-112025333-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025333G>A , CM000673.2:g.112025333G>A GRCh38
NC_000011.9:g.111896057G>A , CM000673.1:g.111896057G>A GRCh37
NC_000011.8:g.111401267G>A NCBI36
NG_013342.1:g.5520G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-140G>A ENSP00000518862.1:n.-140G>A
ENST00000280346.10:c.-140G>A ENSP00000280346.6:n.-140G>A
NM_001931.4:c.-140G>A NP_001922.2:n.-140G>A
Search 100 bp 5'
Search 100 bp 3'