Canonical Allele Identifier: CA1619760082

Gene: PSMB8

Linked Data

• dbSNP Id: rs1582610373
• gnomAD v4: 6-32843139-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843139G>A , CM000668.2:g.32843139G>A	GRCh38
NC_000006.11:g.32810916G>A , CM000668.1:g.32810916G>A	GRCh37
NC_000006.10:g.32918894G>A	NCBI36
NG_009793.3:g.632C>T
NG_028165.1:g.6797C>T
NG_009793.4:g.632C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.169-50C>T
ENST00000697612.1:n.797C>T
ENST00000374881.3:c.136-50C>T	ENSP00000364015.2:n.136-50C>T
ENST00000374882.8:c.148-50C>T MANE Select	ENSP00000364016.4:n.148-50C>T
ENST00000650411.1:n.1419C>T
ENST00000650793.1:n.169-50C>T
ENST00000374881.2:c.136-50C>T	ENSP00000364015.2:n.136-50C>T
ENST00000374882.7:c.148-50C>T	ENSP00000364016.3:n.148-50C>T
ENST00000395339.7:c.148-50C>T	ENSP00000378748.3:n.148-50C>T
ENST00000484003.1:n.374-50C>T
NM_004159.4:c.136-50C>T	NP_004150.1:n.136-50C>T
NM_148919.3:c.148-50C>T	NP_683720.2:n.148-50C>T
NM_148919.4:c.148-50C>T MANE Select	NP_683720.2:n.148-50C>T
NM_004159.5:c.136-50C>T	NP_004150.1:n.136-50C>T