Canonical Allele Identifier: CA1619760033
Gene: PSMB8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843057G= , CM000668.2:g.32843057G= GRCh38
NC_000006.11:g.32810834G= , CM000668.1:g.32810834G= GRCh37
NC_000006.10:g.32918812G= NCBI36
NG_009793.3:g.714C=
NG_028165.1:g.6879C=
NG_009793.4:g.714C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650793.2:n.201C=
ENST00000697612.1:n.879C=
ENST00000374881.3:c.168C= ENSP00000364015.2:p.Asp56=
ENST00000374882.8:c.180C= MANE Select ENSP00000364016.4:p.Asp60=
ENST00000650411.1:n.1501C=
ENST00000650793.1:n.201C=
ENST00000374881.2:c.168C= ENSP00000364015.2:p.Asp56=
ENST00000374882.7:c.180C= ENSP00000364016.3:p.Asp60=
ENST00000395339.7:c.180C= ENSP00000378748.3:p.Asp60=
ENST00000484003.1:n.406C=
NM_004159.4:c.168C= NP_004150.1:p.Asp56=
NM_148919.3:c.180C= NP_683720.2:p.Asp60=
NM_148919.4:c.180C= MANE Select NP_683720.2:p.Asp60=
NM_004159.5:c.168C= NP_004150.1:p.Asp56=