Canonical Allele Identifier: CA1619760028
Gene: PSMB8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843049C= , CM000668.2:g.32843049C= GRCh38
NC_000006.11:g.32810826C= , CM000668.1:g.32810826C= GRCh37
NC_000006.10:g.32918804C= NCBI36
NG_009793.3:g.722G=
NG_028165.1:g.6887G=
NG_009793.4:g.722G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650793.2:n.209G=
ENST00000697612.1:n.887G=
ENST00000374881.3:c.176G= ENSP00000364015.2:p.Arg59=
ENST00000374882.8:c.188G= MANE Select ENSP00000364016.4:p.Arg63=
ENST00000650411.1:n.1509G=
ENST00000650793.1:n.209G=
ENST00000374881.2:c.176G= ENSP00000364015.2:p.Arg59=
ENST00000374882.7:c.188G= ENSP00000364016.3:p.Arg63=
ENST00000395339.7:c.188G= ENSP00000378748.3:p.Arg63=
ENST00000484003.1:n.414G=
NM_004159.4:c.176G= NP_004150.1:p.Arg59=
NM_148919.3:c.188G= NP_683720.2:p.Arg63=
NM_148919.4:c.188G= MANE Select NP_683720.2:p.Arg63=
NM_004159.5:c.176G= NP_004150.1:p.Arg59=