Canonical Allele Identifier: CA449832555

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842731-G-T
• MyVariant Identifiers: chr6:g.32810508G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842731G>T , CM000668.2:g.32842731G>T	GRCh38
NC_000006.11:g.32810508G>T , CM000668.1:g.32810508G>T	GRCh37
NC_000006.10:g.32918486G>T	NCBI36
NG_009793.3:g.1040C>A
NG_028165.1:g.7205C>A
NG_009793.4:g.1040C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.527C>A
ENST00000697612.1:n.1205C>A
ENST00000374881.3:c.336C>A	ENSP00000364015.2:p.Thr112=
ENST00000374882.8:c.348C>A MANE Select	ENSP00000364016.4:p.Thr116=
ENST00000650411.1:n.1669C>A
ENST00000650793.1:n.527C>A
ENST00000374881.2:c.336C>A	ENSP00000364015.2:p.Thr112=
ENST00000374882.7:c.348C>A	ENSP00000364016.3:p.Thr116=
ENST00000395339.7:c.296-20C>A	ENSP00000378748.3:n.296-20C>A
ENST00000484003.1:n.732C>A
NM_004159.4:c.336C>A	NP_004150.1:p.Thr112=
NM_148919.3:c.348C>A	NP_683720.2:p.Thr116=
NM_148919.4:c.348C>A MANE Select	NP_683720.2:p.Thr116=
NM_004159.5:c.336C>A	NP_004150.1:p.Thr112=