Canonical Allele Identifier: CA221874
Gene: DBT HGNC NCBI

Linked Data

ClinVar Variation Id: 93991
dbSNP Id: rs398123660

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100196413G>A , CM000663.2:g.100196413G>A GRCh38
NC_000001.10:g.100661969G>A , CM000663.1:g.100661969G>A GRCh37
NC_000001.9:g.100434557G>A NCBI36
NG_011852.2:g.58441C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000681617.1:c.1417C>T ENSP00000505544.1:p.Arg473Ter
ENST00000681780.1:c.748C>T ENSP00000505780.1:p.Arg250Ter
ENST00000370132.8:c.1291C>T MANE Select ENSP00000359151.3:p.Arg431Ter
NM_001918.3:c.1291C>T NP_001909.3:p.Arg431Ter
XM_005270545.2:c.748C>T XP_005270602.1:p.Arg250Ter
XM_005270546.2:c.748C>T XP_005270603.1:p.Arg250Ter
XM_005270545.4:c.748C>T XP_005270602.1:p.Arg250Ter
XM_017000468.2:c.748C>T XP_016855957.1:p.Arg250Ter
XM_017000469.2:c.748C>T XP_016855958.1:p.Arg250Ter
NM_001918.4:c.1291C>T NP_001909.3:p.Arg431Ter
NM_001918.5:c.1291C>T MANE Select NP_001909.4:p.Arg431Ter
NM_001399969.1:c.748C>T NP_001386898.1:p.Arg250Ter
NM_001399972.1:c.748C>T NP_001386901.1:p.Arg250Ter
NR_174363.1:n.1123C>T
NR_174364.1:n.1464C>T
NR_174365.1:n.1088C>T
NR_174366.1:n.1390C>T