Canonical Allele Identifier: CA2000527648

Gene: DLAT

Linked Data

• dbSNP Id: rs1861924430

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025291T>A , CM000673.2:g.112025291T>A	GRCh38
NC_000011.9:g.111896015T>A , CM000673.1:g.111896015T>A	GRCh37
NC_000011.8:g.111401225T>A	NCBI36
NG_013342.1:g.5478T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-182T>A	ENSP00000518862.1:n.-182T>A
ENST00000280346.10:c.-182T>A	ENSP00000280346.6:n.-182T>A
NM_001931.4:c.-182T>A	NP_001922.2:n.-182T>A