Canonical Allele Identifier: CA969652
Gene: DBT HGNC NCBI

Linked Data

dbSNP Id: rs756058511

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100214950G>A , CM000663.2:g.100214950G>A GRCh38
NC_000001.10:g.100680506G>A , CM000663.1:g.100680506G>A GRCh37
NC_000001.9:g.100453094G>A NCBI36
NG_011852.2:g.39904C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000681617.1:c.806C>T ENSP00000505544.1:p.Ala269Val
ENST00000681780.1:c.263C>T ENSP00000505780.1:p.Ala88Val
ENST00000370131.3:c.806C>T ENSP00000359150.3:p.Ala269Val
ENST00000370132.8:c.806C>T MANE Select ENSP00000359151.3:p.Ala269Val
NM_001918.3:c.806C>T NP_001909.3:p.Ala269Val
XM_005270545.2:c.263C>T XP_005270602.1:p.Ala88Val
XM_005270546.2:c.263C>T XP_005270603.1:p.Ala88Val
XR_946560.1:n.826C>T
XM_005270545.4:c.263C>T XP_005270602.1:p.Ala88Val
XM_017000468.2:c.263C>T XP_016855957.1:p.Ala88Val
XM_017000469.2:c.263C>T XP_016855958.1:p.Ala88Val
XR_946560.3:n.823C>T
NM_001918.4:c.806C>T NP_001909.3:p.Ala269Val
NM_001918.5:c.806C>T MANE Select NP_001909.4:p.Ala269Val
NM_001399969.1:c.263C>T NP_001386898.1:p.Ala88Val
NM_001399972.1:c.263C>T NP_001386901.1:p.Ala88Val
NR_174363.1:n.638C>T
NR_174364.1:n.820C>T
NR_174365.1:n.603C>T
NR_174366.1:n.820C>T