Canonical Allele Identifier: CA1641009993

Gene: BCKDHB

Linked Data

• dbSNP Id: rs1770051216

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80343911T>G , CM000668.2:g.80343911T>G	GRCh38
NC_000006.11:g.81053628T>G , CM000668.1:g.81053628T>G	GRCh37
NC_000006.10:g.81110347T>G	NCBI36
NG_009775.1:g.242285T>G
NG_009775.2:g.242285T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.*107T>G MANE Select	ENSP00000318351.5:n.*107T>G
ENST00000320393.8:c.*107T>G	ENSP00000318351.5:n.*107T>G
ENST00000356489.9:c.*8+99T>G	ENSP00000348880.5:n.*8+99T>G
ENST00000491328.1:n.242+99T>G
NM_000056.3:c.*8+99T>G	NP_000047.1:n.*8+99T>G
NM_183050.2:c.*107T>G	NP_898871.1:n.*107T>G
NM_000056.4:c.*8+99T>G	NP_000047.1:n.*8+99T>G
NM_001318975.1:c.*107T>G	NP_001305904.1:n.*107T>G
NM_183050.3:c.*107T>G	NP_898871.1:n.*107T>G
NR_134945.1:n.1464T>G
XM_011536024.3:c.*292T>G	XP_011534326.1:n.*292T>G
XR_001743546.2:n.1068+70690T>G
XR_001743547.2:n.1068+70690T>G
XR_001743548.2:n.1068+70690T>G
XR_001743549.2:n.1068+70690T>G
XR_002956292.1:n.1068+70690T>G
NM_183050.4:c.*107T>G MANE Select	NP_898871.1:n.*107T>G
NR_134945.2:n.1403T>G
NM_000056.5:c.*8+99T>G	NP_000047.1:n.*8+99T>G