Canonical Allele Identifier: CA671778002
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs1331456422
gnomAD v4: 11-112025325-T-C
MyVariant Identifiers: chr11:g.112025325T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025325T>C , CM000673.2:g.112025325T>C GRCh38
NC_000011.9:g.111896049T>C , CM000673.1:g.111896049T>C GRCh37
NC_000011.8:g.111401259T>C NCBI36
NG_013342.1:g.5512T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-148T>C ENSP00000518862.1:n.-148T>C
ENST00000280346.10:c.-148T>C ENSP00000280346.6:n.-148T>C
NM_001931.4:c.-148T>C NP_001922.2:n.-148T>C
Search 100 bp 5'
Search 100 bp 3'