Canonical Allele Identifier: CA2678184398

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842655-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842655T>C , CM000668.2:g.32842655T>C	GRCh38
NC_000006.11:g.32810432T>C , CM000668.1:g.32810432T>C	GRCh37
NC_000006.10:g.32918410T>C	NCBI36
NG_009793.3:g.1116A>G
NG_028165.1:g.7281A>G
NG_009793.4:g.1116A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.603A>G
ENST00000697612.1:n.1264+17A>G
ENST00000374881.3:c.395+17A>G	ENSP00000364015.2:n.395+17A>G
ENST00000374882.8:c.407+17A>G MANE Select	ENSP00000364016.4:n.407+17A>G
ENST00000650411.1:n.1728+17A>G
ENST00000650793.1:n.603A>G
ENST00000374881.2:c.395+17A>G	ENSP00000364015.2:n.395+17A>G
ENST00000374882.7:c.407+17A>G	ENSP00000364016.3:n.407+17A>G
ENST00000395339.7:c.335+17A>G	ENSP00000378748.3:n.335+17A>G
ENST00000484003.1:n.791+17A>G
NM_004159.4:c.395+17A>G	NP_004150.1:n.395+17A>G
NM_148919.3:c.407+17A>G	NP_683720.2:n.407+17A>G
NM_148919.4:c.407+17A>G MANE Select	NP_683720.2:n.407+17A>G
NM_004159.5:c.395+17A>G	NP_004150.1:n.395+17A>G