Canonical Allele Identifier: CA2679496937
Gene: BCKDHB HGNC NCBI

Linked Data

gnomAD v4: 6-80106650-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80106650C>A , CM000668.2:g.80106650C>A GRCh38
NC_000006.11:g.80816367C>A , CM000668.1:g.80816367C>A GRCh37
NC_000006.10:g.80873086C>A NCBI36
NG_009775.1:g.5024C>A
NG_009775.2:g.5024C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.8:c.-44C>A ENSP00000318351.5:n.-44C>A
ENST00000356489.9:c.-44C>A ENSP00000348880.5:n.-44C>A
ENST00000369760.8:c.-44C>A ENSP00000358775.4:n.-44C>A
NM_000056.3:c.-44C>A NP_000047.1:n.-44C>A
NM_183050.2:c.-44C>A NP_898871.1:n.-44C>A
XM_006715542.2:c.-48C>A XP_006715605.1:n.-48C>A
NM_000056.4:c.-44C>A NP_000047.1:n.-44C>A
NM_001318975.1:c.-48C>A NP_001305904.1:n.-48C>A
NM_183050.3:c.-44C>A NP_898871.1:n.-44C>A
NR_134945.1:n.41C>A