Canonical Allele Identifier: CA671778015

Gene: DLAT

Linked Data

• dbSNP Id: rs1167510285
• gnomAD v3: 11-112025341-T-C
• gnomAD v4: 11-112025341-T-C
• MyVariant Identifiers: chr11:g.112025341T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025341T>C , CM000673.2:g.112025341T>C	GRCh38
NC_000011.9:g.111896065T>C , CM000673.1:g.111896065T>C	GRCh37
NC_000011.8:g.111401275T>C	NCBI36
NG_013342.1:g.5528T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-132T>C	ENSP00000518862.1:n.-132T>C
ENST00000280346.10:c.-132T>C	ENSP00000280346.6:n.-132T>C
NM_001931.4:c.-132T>C	NP_001922.2:n.-132T>C