Canonical Allele Identifier: CA2578579573

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842792-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842792A>C , CM000668.2:g.32842792A>C	GRCh38
NC_000006.11:g.32810569A>C , CM000668.1:g.32810569A>C	GRCh37
NC_000006.10:g.32918547A>C	NCBI36
NG_009793.3:g.979T>G
NG_028165.1:g.7144T>G
NG_009793.4:g.979T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.466T>G
ENST00000697612.1:n.1144T>G
ENST00000374881.3:c.284-9T>G	ENSP00000364015.2:n.284-9T>G
ENST00000374882.8:c.296-9T>G MANE Select	ENSP00000364016.4:n.296-9T>G
ENST00000650411.1:n.1617-9T>G
ENST00000650793.1:n.466T>G
ENST00000374881.2:c.284-9T>G	ENSP00000364015.2:n.284-9T>G
ENST00000374882.7:c.296-9T>G	ENSP00000364016.3:n.296-9T>G
ENST00000395339.7:c.296-81T>G	ENSP00000378748.3:n.296-81T>G
ENST00000484003.1:n.671T>G
NM_004159.4:c.284-9T>G	NP_004150.1:n.284-9T>G
NM_148919.3:c.296-9T>G	NP_683720.2:n.296-9T>G
NM_148919.4:c.296-9T>G MANE Select	NP_683720.2:n.296-9T>G
NM_004159.5:c.284-9T>G	NP_004150.1:n.284-9T>G