Canonical Allele Identifier: CA228541392
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs782226186

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025348A>C , CM000673.2:g.112025348A>C GRCh38
NC_000011.9:g.111896072A>C , CM000673.1:g.111896072A>C GRCh37
NC_000011.8:g.111401282A>C NCBI36
NG_013342.1:g.5535A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-125A>C ENSP00000518862.1:n.-125A>C
ENST00000280346.10:c.-125A>C ENSP00000280346.6:n.-125A>C
NM_001931.4:c.-125A>C NP_001922.2:n.-125A>C