Canonical Allele Identifier: CA3902499
Gene: BCKDHB HGNC NCBI

Linked Data

dbSNP Id: rs751941303
gnomAD v2: 6-80816520-A-C
gnomAD v3: 6-80106803-A-C
gnomAD v4: 6-80106803-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80106803A>C , CM000668.2:g.80106803A>C GRCh38
NC_000006.11:g.80816520A>C , CM000668.1:g.80816520A>C GRCh37
NC_000006.10:g.80873239A>C NCBI36
NG_009775.1:g.5177A>C
NG_009775.2:g.5177A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.110A>C MANE Select ENSP00000318351.5:p.His37Pro
ENST00000320393.8:c.110A>C ENSP00000318351.5:p.His37Pro
ENST00000356489.9:c.110A>C ENSP00000348880.5:p.His37Pro
ENST00000369760.8:c.110A>C ENSP00000358775.4:p.His37Pro
NM_000056.3:c.110A>C NP_000047.1:p.His37Pro
NM_183050.2:c.110A>C NP_898871.1:p.His37Pro
XM_005248756.3:c.110A>C XP_005248813.1:p.His37Pro
XM_006715542.2:c.-15+120A>C XP_006715605.1:n.-15+120A>C
XM_011536023.1:c.110A>C XP_011534325.1:p.His37Pro
XM_011536024.1:c.110A>C XP_011534326.1:p.His37Pro
XM_011536025.1:c.110A>C XP_011534327.1:p.His37Pro
XM_011536027.1:c.110A>C XP_011534329.1:p.His37Pro
NM_000056.4:c.110A>C NP_000047.1:p.His37Pro
NM_001318975.1:c.-15+120A>C NP_001305904.1:n.-15+120A>C
NM_183050.3:c.110A>C NP_898871.1:p.His37Pro
NR_134945.1:n.194A>C
XM_005248756.5:c.110A>C XP_005248813.1:p.His37Pro
XM_011536023.3:c.110A>C XP_011534325.1:p.His37Pro
XM_011536024.3:c.110A>C XP_011534326.1:p.His37Pro
XM_011536025.3:c.110A>C XP_011534327.1:p.His37Pro
XR_001743546.2:n.140A>C
XR_001743547.2:n.140A>C
XR_001743548.2:n.140A>C
XR_001743549.2:n.140A>C
XR_002956292.1:n.140A>C
NM_183050.4:c.110A>C MANE Select NP_898871.1:p.His37Pro
NR_134945.2:n.133A>C
NM_000056.5:c.110A>C NP_000047.1:p.His37Pro