Canonical Allele Identifier: CA2678184913

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32843138-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843138A>C , CM000668.2:g.32843138A>C	GRCh38
NC_000006.11:g.32810915A>C , CM000668.1:g.32810915A>C	GRCh37
NC_000006.10:g.32918893A>C	NCBI36
NG_009793.3:g.633T>G
NG_028165.1:g.6798T>G
NG_009793.4:g.633T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.169-49T>G
ENST00000697612.1:n.798T>G
ENST00000374881.3:c.136-49T>G	ENSP00000364015.2:n.136-49T>G
ENST00000374882.8:c.148-49T>G MANE Select	ENSP00000364016.4:n.148-49T>G
ENST00000650411.1:n.1420T>G
ENST00000650793.1:n.169-49T>G
ENST00000374881.2:c.136-49T>G	ENSP00000364015.2:n.136-49T>G
ENST00000374882.7:c.148-49T>G	ENSP00000364016.3:n.148-49T>G
ENST00000395339.7:c.148-49T>G	ENSP00000378748.3:n.148-49T>G
ENST00000484003.1:n.374-49T>G
NM_004159.4:c.136-49T>G	NP_004150.1:n.136-49T>G
NM_148919.3:c.148-49T>G	NP_683720.2:n.148-49T>G
NM_148919.4:c.148-49T>G MANE Select	NP_683720.2:n.148-49T>G
NM_004159.5:c.136-49T>G	NP_004150.1:n.136-49T>G