Canonical Allele Identifier: CA363589456
Gene: PSMB8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843010A>T , CM000668.2:g.32843010A>T GRCh38
NC_000006.11:g.32810787A>T , CM000668.1:g.32810787A>T GRCh37
NC_000006.10:g.32918765A>T NCBI36
NG_009793.3:g.761T>A
NG_028165.1:g.6926T>A
NG_009793.4:g.761T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.248T>A
ENST00000697612.1:n.926T>A
ENST00000374881.3:c.215T>A ENSP00000364015.2:p.Leu72His
ENST00000374882.8:c.227T>A MANE Select ENSP00000364016.4:p.Leu76His
ENST00000650411.1:n.1548T>A
ENST00000650793.1:n.248T>A
ENST00000374881.2:c.215T>A ENSP00000364015.2:p.Leu72His
ENST00000374882.7:c.227T>A ENSP00000364016.3:p.Leu76His
ENST00000395339.7:c.227T>A ENSP00000378748.3:p.Leu76His
ENST00000484003.1:n.453T>A
NM_004159.4:c.215T>A NP_004150.1:p.Leu72His
NM_148919.3:c.227T>A NP_683720.2:p.Leu76His
NM_148919.4:c.227T>A MANE Select NP_683720.2:p.Leu76His
NM_004159.5:c.215T>A NP_004150.1:p.Leu72His