Canonical Allele Identifier: CA828530180

Gene: BCKDHB

Linked Data

• dbSNP Id: rs1364170450
• gnomAD v3: 6-80106692-G-C
• gnomAD v4: 6-80106692-G-C
• MyVariant Identifiers: chr6:g.80816409G>C (hg19) ; chr6:g.80106692G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80106692G>C , CM000668.2:g.80106692G>C	GRCh38
NC_000006.11:g.80816409G>C , CM000668.1:g.80816409G>C	GRCh37
NC_000006.10:g.80873128G>C	NCBI36
NG_009775.1:g.5066G>C
NG_009775.2:g.5066G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000320393.9:c.-2G>C MANE Select	ENSP00000318351.5:n.-2G>C
ENST00000320393.8:c.-2G>C	ENSP00000318351.5:n.-2G>C
ENST00000356489.9:c.-2G>C	ENSP00000348880.5:n.-2G>C
ENST00000369760.8:c.-2G>C	ENSP00000358775.4:n.-2G>C
NM_000056.3:c.-2G>C	NP_000047.1:n.-2G>C
NM_183050.2:c.-2G>C	NP_898871.1:n.-2G>C
XM_005248756.3:c.-2G>C	XP_005248813.1:n.-2G>C
XM_006715542.2:c.-15+9G>C	XP_006715605.1:n.-15+9G>C
XM_011536023.1:c.-2G>C	XP_011534325.1:n.-2G>C
XM_011536024.1:c.-2G>C	XP_011534326.1:n.-2G>C
XM_011536025.1:c.-2G>C	XP_011534327.1:n.-2G>C
XM_011536027.1:c.-2G>C	XP_011534329.1:n.-2G>C
NM_000056.4:c.-2G>C	NP_000047.1:n.-2G>C
NM_001318975.1:c.-15+9G>C	NP_001305904.1:n.-15+9G>C
NM_183050.3:c.-2G>C	NP_898871.1:n.-2G>C
NR_134945.1:n.83G>C
XM_005248756.5:c.-2G>C	XP_005248813.1:n.-2G>C
XM_011536023.3:c.-2G>C	XP_011534325.1:n.-2G>C
XM_011536024.3:c.-2G>C	XP_011534326.1:n.-2G>C
XM_011536025.3:c.-2G>C	XP_011534327.1:n.-2G>C
XR_001743546.2:n.29G>C
XR_001743547.2:n.29G>C
XR_001743548.2:n.29G>C
XR_001743549.2:n.29G>C
XR_002956292.1:n.29G>C
NM_183050.4:c.-2G>C MANE Select	NP_898871.1:n.-2G>C
NR_134945.2:n.22G>C
NM_000056.5:c.-2G>C	NP_000047.1:n.-2G>C