Canonical Allele Identifier: CA364658135
Gene: BCKDHB HGNC NCBI

Linked Data

dbSNP Id: rs768452867
gnomAD v2: 6-80816493-G-T
gnomAD v3: 6-80106776-G-T
gnomAD v4: 6-80106776-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80106776G>T , CM000668.2:g.80106776G>T GRCh38
NC_000006.11:g.80816493G>T , CM000668.1:g.80816493G>T GRCh37
NC_000006.10:g.80873212G>T NCBI36
NG_009775.1:g.5150G>T
NG_009775.2:g.5150G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.83G>T MANE Select ENSP00000318351.5:p.Gly28Val
ENST00000320393.8:c.83G>T ENSP00000318351.5:p.Gly28Val
ENST00000356489.9:c.83G>T ENSP00000348880.5:p.Gly28Val
ENST00000369760.8:c.83G>T ENSP00000358775.4:p.Gly28Val
NM_000056.3:c.83G>T NP_000047.1:p.Gly28Val
NM_183050.2:c.83G>T NP_898871.1:p.Gly28Val
XM_005248756.3:c.83G>T XP_005248813.1:p.Gly28Val
XM_006715542.2:c.-15+93G>T XP_006715605.1:n.-15+93G>T
XM_011536023.1:c.83G>T XP_011534325.1:p.Gly28Val
XM_011536024.1:c.83G>T XP_011534326.1:p.Gly28Val
XM_011536025.1:c.83G>T XP_011534327.1:p.Gly28Val
XM_011536027.1:c.83G>T XP_011534329.1:p.Gly28Val
NM_000056.4:c.83G>T NP_000047.1:p.Gly28Val
NM_001318975.1:c.-15+93G>T NP_001305904.1:n.-15+93G>T
NM_183050.3:c.83G>T NP_898871.1:p.Gly28Val
NR_134945.1:n.167G>T
XM_005248756.5:c.83G>T XP_005248813.1:p.Gly28Val
XM_011536023.3:c.83G>T XP_011534325.1:p.Gly28Val
XM_011536024.3:c.83G>T XP_011534326.1:p.Gly28Val
XM_011536025.3:c.83G>T XP_011534327.1:p.Gly28Val
XR_001743546.2:n.113G>T
XR_001743547.2:n.113G>T
XR_001743548.2:n.113G>T
XR_001743549.2:n.113G>T
XR_002956292.1:n.113G>T
NM_183050.4:c.83G>T MANE Select NP_898871.1:p.Gly28Val
NR_134945.2:n.106G>T
NM_000056.5:c.83G>T NP_000047.1:p.Gly28Val