Canonical Allele Identifier: CA1619760025
Gene: PSMB8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843046T= , CM000668.2:g.32843046T= GRCh38
NC_000006.11:g.32810823T= , CM000668.1:g.32810823T= GRCh37
NC_000006.10:g.32918801T= NCBI36
NG_009793.3:g.725A=
NG_028165.1:g.6890A=
NG_009793.4:g.725A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650793.2:n.212A=
ENST00000697612.1:n.890A=
ENST00000374881.3:c.179A= ENSP00000364015.2:p.Asn60=
ENST00000374882.8:c.191A= MANE Select ENSP00000364016.4:p.Asn64=
ENST00000650411.1:n.1512A=
ENST00000650793.1:n.212A=
ENST00000374881.2:c.179A= ENSP00000364015.2:p.Asn60=
ENST00000374882.7:c.191A= ENSP00000364016.3:p.Asn64=
ENST00000395339.7:c.191A= ENSP00000378748.3:p.Asn64=
ENST00000484003.1:n.417A=
NM_004159.4:c.179A= NP_004150.1:p.Asn60=
NM_148919.3:c.191A= NP_683720.2:p.Asn64=
NM_148919.4:c.191A= MANE Select NP_683720.2:p.Asn64=
NM_004159.5:c.179A= NP_004150.1:p.Asn60=