Canonical Allele Identifier: CA363589059
Gene: PSMB8 HGNC NCBI

Linked Data

gnomAD v4: 6-32842673-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32842673T>C , CM000668.2:g.32842673T>C GRCh38
NC_000006.11:g.32810450T>C , CM000668.1:g.32810450T>C GRCh37
NC_000006.10:g.32918428T>C NCBI36
NG_009793.3:g.1098A>G
NG_028165.1:g.7263A>G
NG_009793.4:g.1098A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.585A>G
ENST00000697612.1:n.1263A>G
ENST00000374881.3:c.394A>G ENSP00000364015.2:p.Arg132Gly
ENST00000374882.8:c.406A>G MANE Select ENSP00000364016.4:p.Arg136Gly
ENST00000650411.1:n.1727A>G
ENST00000650793.1:n.585A>G
ENST00000374881.2:c.394A>G ENSP00000364015.2:p.Arg132Gly
ENST00000374882.7:c.406A>G ENSP00000364016.3:p.Arg136Gly
ENST00000395339.7:c.334A>G ENSP00000378748.3:p.Arg112Gly
ENST00000484003.1:n.790A>G
NM_004159.4:c.394A>G NP_004150.1:p.Arg132Gly
NM_148919.3:c.406A>G NP_683720.2:p.Arg136Gly
NM_148919.4:c.406A>G MANE Select NP_683720.2:p.Arg136Gly
NM_004159.5:c.394A>G NP_004150.1:p.Arg132Gly