Canonical Allele Identifier: CA363589336

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842951-A-T
• MyVariant Identifiers: chr6:g.32810728A>T (hg19) ; chr6:g.32842951A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842951A>T , CM000668.2:g.32842951A>T	GRCh38
NC_000006.11:g.32810728A>T , CM000668.1:g.32810728A>T	GRCh37
NC_000006.10:g.32918706A>T	NCBI36
NG_009793.3:g.820T>A
NG_028165.1:g.6985T>A
NG_009793.4:g.820T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.307T>A
ENST00000697612.1:n.985T>A
ENST00000374881.3:c.274T>A	ENSP00000364015.2:p.Ser92Thr
ENST00000374882.8:c.286T>A MANE Select	ENSP00000364016.4:p.Ser96Thr
ENST00000650411.1:n.1607T>A
ENST00000650793.1:n.307T>A
ENST00000374881.2:c.274T>A	ENSP00000364015.2:p.Ser92Thr
ENST00000374882.7:c.286T>A	ENSP00000364016.3:p.Ser96Thr
ENST00000395339.7:c.286T>A	ENSP00000378748.3:p.Ser96Thr
ENST00000484003.1:n.512T>A
NM_004159.4:c.274T>A	NP_004150.1:p.Ser92Thr
NM_148919.3:c.286T>A	NP_683720.2:p.Ser96Thr
NM_148919.4:c.286T>A MANE Select	NP_683720.2:p.Ser96Thr
NM_004159.5:c.274T>A	NP_004150.1:p.Ser92Thr