Canonical Allele Identifier: CA363589436
Gene: PSMB8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843001T>C , CM000668.2:g.32843001T>C GRCh38
NC_000006.11:g.32810778T>C , CM000668.1:g.32810778T>C GRCh37
NC_000006.10:g.32918756T>C NCBI36
NG_009793.3:g.770A>G
NG_028165.1:g.6935A>G
NG_009793.4:g.770A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.257A>G
ENST00000697612.1:n.935A>G
ENST00000374881.3:c.224A>G ENSP00000364015.2:p.Lys75Arg
ENST00000374882.8:c.236A>G MANE Select ENSP00000364016.4:p.Lys79Arg
ENST00000650411.1:n.1557A>G
ENST00000650793.1:n.257A>G
ENST00000374881.2:c.224A>G ENSP00000364015.2:p.Lys75Arg
ENST00000374882.7:c.236A>G ENSP00000364016.3:p.Lys79Arg
ENST00000395339.7:c.236A>G ENSP00000378748.3:p.Lys79Arg
ENST00000484003.1:n.462A>G
NM_004159.4:c.224A>G NP_004150.1:p.Lys75Arg
NM_148919.3:c.236A>G NP_683720.2:p.Lys79Arg
NM_148919.4:c.236A>G MANE Select NP_683720.2:p.Lys79Arg
NM_004159.5:c.224A>G NP_004150.1:p.Lys75Arg