Canonical Allele Identifier: CA2679496942

Gene: BCKDHB

Linked Data

• gnomAD v4: 6-80106655-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80106655T>A , CM000668.2:g.80106655T>A	GRCh38
NC_000006.11:g.80816372T>A , CM000668.1:g.80816372T>A	GRCh37
NC_000006.10:g.80873091T>A	NCBI36
NG_009775.1:g.5029T>A
NG_009775.2:g.5029T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.8:c.-39T>A	ENSP00000318351.5:n.-39T>A
ENST00000356489.9:c.-39T>A	ENSP00000348880.5:n.-39T>A
ENST00000369760.8:c.-39T>A	ENSP00000358775.4:n.-39T>A
NM_000056.3:c.-39T>A	NP_000047.1:n.-39T>A
NM_183050.2:c.-39T>A	NP_898871.1:n.-39T>A
XM_006715542.2:c.-43T>A	XP_006715605.1:n.-43T>A
NM_000056.4:c.-39T>A	NP_000047.1:n.-39T>A
NM_001318975.1:c.-43T>A	NP_001305904.1:n.-43T>A
NM_183050.3:c.-39T>A	NP_898871.1:n.-39T>A
NR_134945.1:n.46T>A