Canonical Allele Identifier: CA364657729

Gene: BCKDHB

Linked Data

• dbSNP Id: rs1402705633
• gnomAD v2: 6-80878611-A-C
• gnomAD v4: 6-80168894-A-C
• MyVariant Identifiers: chr6:g.80878611A>C (hg19) ; chr6:g.80168894A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168894A>C , CM000668.2:g.80168894A>C	GRCh38
NC_000006.11:g.80878611A>C , CM000668.1:g.80878611A>C	GRCh37
NC_000006.10:g.80935330A>C	NCBI36
NG_009775.1:g.67268A>C
NG_009775.2:g.67268A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.497A>C MANE Select	ENSP00000318351.5:p.Lys166Thr
ENST00000320393.8:c.497A>C	ENSP00000318351.5:p.Lys166Thr
ENST00000356489.9:c.497A>C	ENSP00000348880.5:p.Lys166Thr
ENST00000369760.8:c.497A>C	ENSP00000358775.4:p.Lys166Thr
NM_000056.3:c.497A>C	NP_000047.1:p.Lys166Thr
NM_183050.2:c.497A>C	NP_898871.1:p.Lys166Thr
XM_005248756.3:c.497A>C	XP_005248813.1:p.Lys166Thr
XM_006715542.2:c.287A>C	XP_006715605.1:p.Lys96Thr
XM_011536023.1:c.497A>C	XP_011534325.1:p.Lys166Thr
XM_011536024.1:c.497A>C	XP_011534326.1:p.Lys166Thr
XM_011536025.1:c.497A>C	XP_011534327.1:p.Lys166Thr
XM_011536026.1:c.287A>C	XP_011534328.1:p.Lys96Thr
XM_011536027.1:c.497A>C	XP_011534329.1:p.Lys166Thr
NM_000056.4:c.497A>C	NP_000047.1:p.Lys166Thr
NM_001318975.1:c.287A>C	NP_001305904.1:p.Lys96Thr
NM_183050.3:c.497A>C	NP_898871.1:p.Lys166Thr
NR_134945.1:n.581A>C
XM_005248756.5:c.497A>C	XP_005248813.1:p.Lys166Thr
XM_011536023.3:c.497A>C	XP_011534325.1:p.Lys166Thr
XM_011536024.3:c.497A>C	XP_011534326.1:p.Lys166Thr
XM_011536025.3:c.497A>C	XP_011534327.1:p.Lys166Thr
XR_001743546.2:n.527A>C
XR_001743547.2:n.527A>C
XR_001743548.2:n.527A>C
XR_001743549.2:n.527A>C
XR_002956292.1:n.527A>C
NM_183050.4:c.497A>C MANE Select	NP_898871.1:p.Lys166Thr
NR_134945.2:n.520A>C
NM_000056.5:c.497A>C	NP_000047.1:p.Lys166Thr