Canonical Allele Identifier: CA363589352

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810737A>T (hg19) ; chr6:g.32842960A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842960A>T , CM000668.2:g.32842960A>T	GRCh38
NC_000006.11:g.32810737A>T , CM000668.1:g.32810737A>T	GRCh37
NC_000006.10:g.32918715A>T	NCBI36
NG_009793.3:g.811T>A
NG_028165.1:g.6976T>A
NG_009793.4:g.811T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.298T>A
ENST00000697612.1:n.976T>A
ENST00000374881.3:c.265T>A	ENSP00000364015.2:p.Ser89Thr
ENST00000374882.8:c.277T>A MANE Select	ENSP00000364016.4:p.Ser93Thr
ENST00000650411.1:n.1598T>A
ENST00000650793.1:n.298T>A
ENST00000374881.2:c.265T>A	ENSP00000364015.2:p.Ser89Thr
ENST00000374882.7:c.277T>A	ENSP00000364016.3:p.Ser93Thr
ENST00000395339.7:c.277T>A	ENSP00000378748.3:p.Ser93Thr
ENST00000484003.1:n.503T>A
NM_004159.4:c.265T>A	NP_004150.1:p.Ser89Thr
NM_148919.3:c.277T>A	NP_683720.2:p.Ser93Thr
NM_148919.4:c.277T>A MANE Select	NP_683720.2:p.Ser93Thr
NM_004159.5:c.265T>A	NP_004150.1:p.Ser89Thr