Canonical Allele Identifier: CA1619760027
Gene: PSMB8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843048C= , CM000668.2:g.32843048C= GRCh38
NC_000006.11:g.32810825C= , CM000668.1:g.32810825C= GRCh37
NC_000006.10:g.32918803C= NCBI36
NG_009793.3:g.723G=
NG_028165.1:g.6888G=
NG_009793.4:g.723G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650793.2:n.210G=
ENST00000697612.1:n.888G=
ENST00000374881.3:c.177G= ENSP00000364015.2:p.Arg59=
ENST00000374882.8:c.189G= MANE Select ENSP00000364016.4:p.Arg63=
ENST00000650411.1:n.1510G=
ENST00000650793.1:n.210G=
ENST00000374881.2:c.177G= ENSP00000364015.2:p.Arg59=
ENST00000374882.7:c.189G= ENSP00000364016.3:p.Arg63=
ENST00000395339.7:c.189G= ENSP00000378748.3:p.Arg63=
ENST00000484003.1:n.415G=
NM_004159.4:c.177G= NP_004150.1:p.Arg59=
NM_148919.3:c.189G= NP_683720.2:p.Arg63=
NM_148919.4:c.189G= MANE Select NP_683720.2:p.Arg63=
NM_004159.5:c.177G= NP_004150.1:p.Arg59=