Canonical Allele Identifier: CA2678184374

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842625-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842625G>T , CM000668.2:g.32842625G>T	GRCh38
NC_000006.11:g.32810402G>T , CM000668.1:g.32810402G>T	GRCh37
NC_000006.10:g.32918380G>T	NCBI36
NG_009793.3:g.1146C>A
NG_028165.1:g.7311C>A
NG_009793.4:g.1146C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.633C>A
ENST00000697612.1:n.1264+47C>A
ENST00000374881.3:c.395+47C>A	ENSP00000364015.2:n.395+47C>A
ENST00000374882.8:c.407+47C>A MANE Select	ENSP00000364016.4:n.407+47C>A
ENST00000650411.1:n.1728+47C>A
ENST00000650793.1:n.633C>A
ENST00000374881.2:c.395+47C>A	ENSP00000364015.2:n.395+47C>A
ENST00000374882.7:c.407+47C>A	ENSP00000364016.3:n.407+47C>A
ENST00000395339.7:c.335+47C>A	ENSP00000378748.3:n.335+47C>A
ENST00000484003.1:n.791+47C>A
NM_004159.4:c.395+47C>A	NP_004150.1:n.395+47C>A
NM_148919.3:c.407+47C>A	NP_683720.2:n.407+47C>A
NM_148919.4:c.407+47C>A MANE Select	NP_683720.2:n.407+47C>A
NM_004159.5:c.395+47C>A	NP_004150.1:n.395+47C>A