Canonical Allele Identifier: CA3902484

Gene: BCKDHB

Linked Data

• ClinVar Variation Id: 358168
• ClinVar RCV Id: RCV000324921 ; RCV000419989 ; RCV001727704 ; RCV001835785
• dbSNP Id: rs376293687
• ExAC: 6:80816461 A / G
• gnomAD v2: 6-80816461-A-G
• gnomAD v3: 6-80106744-A-G
• gnomAD v4: 6-80106744-A-G
• MyVariant Identifiers: chr6:g.80816461A>G (hg19) ; chr6:g.80106744A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80106744A>G , CM000668.2:g.80106744A>G	GRCh38
NC_000006.11:g.80816461A>G , CM000668.1:g.80816461A>G	GRCh37
NC_000006.10:g.80873180A>G	NCBI36
NG_009775.1:g.5118A>G
NG_009775.2:g.5118A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.51A>G MANE Select	ENSP00000318351.5:p.Ala17=
ENST00000320393.8:c.51A>G	ENSP00000318351.5:p.Ala17=
ENST00000356489.9:c.51A>G	ENSP00000348880.5:p.Ala17=
ENST00000369760.8:c.51A>G	ENSP00000358775.4:p.Ala17=
NM_000056.3:c.51A>G	NP_000047.1:p.Ala17=
NM_183050.2:c.51A>G	NP_898871.1:p.Ala17=
XM_005248756.3:c.51A>G	XP_005248813.1:p.Ala17=
XM_006715542.2:c.-15+61A>G	XP_006715605.1:n.-15+61A>G
XM_011536023.1:c.51A>G	XP_011534325.1:p.Ala17=
XM_011536024.1:c.51A>G	XP_011534326.1:p.Ala17=
XM_011536025.1:c.51A>G	XP_011534327.1:p.Ala17=
XM_011536027.1:c.51A>G	XP_011534329.1:p.Ala17=
NM_000056.4:c.51A>G	NP_000047.1:p.Ala17=
NM_001318975.1:c.-15+61A>G	NP_001305904.1:n.-15+61A>G
NM_183050.3:c.51A>G	NP_898871.1:p.Ala17=
NR_134945.1:n.135A>G
XM_005248756.5:c.51A>G	XP_005248813.1:p.Ala17=
XM_011536023.3:c.51A>G	XP_011534325.1:p.Ala17=
XM_011536024.3:c.51A>G	XP_011534326.1:p.Ala17=
XM_011536025.3:c.51A>G	XP_011534327.1:p.Ala17=
XR_001743546.2:n.81A>G
XR_001743547.2:n.81A>G
XR_001743548.2:n.81A>G
XR_001743549.2:n.81A>G
XR_002956292.1:n.81A>G
NM_183050.4:c.51A>G MANE Select	NP_898871.1:p.Ala17=
NR_134945.2:n.74A>G
NM_000056.5:c.51A>G	NP_000047.1:p.Ala17=