Canonical Allele Identifier: CA1641009885

Gene: BCKDHB

Linked Data

• dbSNP Id: rs1770046647

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80343822C>T , CM000668.2:g.80343822C>T	GRCh38
NC_000006.11:g.81053539C>T , CM000668.1:g.81053539C>T	GRCh37
NC_000006.10:g.81110258C>T	NCBI36
NG_009775.1:g.242196C>T
NG_009775.2:g.242196C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.*18C>T MANE Select	ENSP00000318351.5:n.*18C>T
ENST00000320393.8:c.*18C>T	ENSP00000318351.5:n.*18C>T
ENST00000356489.9:c.*8+10C>T	ENSP00000348880.5:n.*8+10C>T
ENST00000491328.1:n.242+10C>T
NM_000056.3:c.*8+10C>T	NP_000047.1:n.*8+10C>T
NM_183050.2:c.*18C>T	NP_898871.1:n.*18C>T
NM_000056.4:c.*8+10C>T	NP_000047.1:n.*8+10C>T
NM_001318975.1:c.*18C>T	NP_001305904.1:n.*18C>T
NM_183050.3:c.*18C>T	NP_898871.1:n.*18C>T
NR_134945.1:n.1375C>T
XM_011536024.3:c.*203C>T	XP_011534326.1:n.*203C>T
XR_001743546.2:n.1068+70601C>T
XR_001743547.2:n.1068+70601C>T
XR_001743548.2:n.1068+70601C>T
XR_001743549.2:n.1068+70601C>T
XR_002956292.1:n.1068+70601C>T
NM_183050.4:c.*18C>T MANE Select	NP_898871.1:n.*18C>T
NR_134945.2:n.1314C>T
NM_000056.5:c.*8+10C>T	NP_000047.1:n.*8+10C>T