Canonical Allele Identifier: CA363589555
Gene: PSMB8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843058T>A , CM000668.2:g.32843058T>A GRCh38
NC_000006.11:g.32810835T>A , CM000668.1:g.32810835T>A GRCh37
NC_000006.10:g.32918813T>A NCBI36
NG_009793.3:g.713A>T
NG_028165.1:g.6878A>T
NG_009793.4:g.713A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.200A>T
ENST00000697612.1:n.878A>T
ENST00000374881.3:c.167A>T ENSP00000364015.2:p.Asp56Val
ENST00000374882.8:c.179A>T MANE Select ENSP00000364016.4:p.Asp60Val
ENST00000650411.1:n.1500A>T
ENST00000650793.1:n.200A>T
ENST00000374881.2:c.167A>T ENSP00000364015.2:p.Asp56Val
ENST00000374882.7:c.179A>T ENSP00000364016.3:p.Asp60Val
ENST00000395339.7:c.179A>T ENSP00000378748.3:p.Asp60Val
ENST00000484003.1:n.405A>T
NM_004159.4:c.167A>T NP_004150.1:p.Asp56Val
NM_148919.3:c.179A>T NP_683720.2:p.Asp60Val
NM_148919.4:c.179A>T MANE Select NP_683720.2:p.Asp60Val
NM_004159.5:c.167A>T NP_004150.1:p.Asp56Val