Canonical Allele Identifier: CA671778013

Gene: DLAT

Linked Data

• dbSNP Id: rs946920655
• gnomAD v3: 11-112025337-C-G
• gnomAD v4: 11-112025337-C-G
• MyVariant Identifiers: chr11:g.112025337C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025337C>G , CM000673.2:g.112025337C>G	GRCh38
NC_000011.9:g.111896061C>G , CM000673.1:g.111896061C>G	GRCh37
NC_000011.8:g.111401271C>G	NCBI36
NG_013342.1:g.5524C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-136C>G	ENSP00000518862.1:n.-136C>G
ENST00000280346.10:c.-136C>G	ENSP00000280346.6:n.-136C>G
NM_001931.4:c.-136C>G	NP_001922.2:n.-136C>G