Canonical Allele Identifier: CA2615976992
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs2137673081

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025306C>T , CM000673.2:g.112025306C>T GRCh38
NC_000011.9:g.111896030C>T , CM000673.1:g.111896030C>T GRCh37
NC_000011.8:g.111401240C>T NCBI36
NG_013342.1:g.5493C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-167C>T ENSP00000518862.1:n.-167C>T
ENST00000280346.10:c.-167C>T ENSP00000280346.6:n.-167C>T
NM_001931.4:c.-167C>T NP_001922.2:n.-167C>T