Canonical Allele Identifier: CA363589177

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810503G>T (hg19) ; chr6:g.32842726G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842726G>T , CM000668.2:g.32842726G>T	GRCh38
NC_000006.11:g.32810503G>T , CM000668.1:g.32810503G>T	GRCh37
NC_000006.10:g.32918481G>T	NCBI36
NG_009793.3:g.1045C>A
NG_028165.1:g.7210C>A
NG_009793.4:g.1045C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.532C>A
ENST00000697612.1:n.1210C>A
ENST00000374881.3:c.341C>A	ENSP00000364015.2:p.Ser114Tyr
ENST00000374882.8:c.353C>A MANE Select	ENSP00000364016.4:p.Ser118Tyr
ENST00000650411.1:n.1674C>A
ENST00000650793.1:n.532C>A
ENST00000374881.2:c.341C>A	ENSP00000364015.2:p.Ser114Tyr
ENST00000374882.7:c.353C>A	ENSP00000364016.3:p.Ser118Tyr
ENST00000395339.7:c.296-15C>A	ENSP00000378748.3:n.296-15C>A
ENST00000484003.1:n.737C>A
NM_004159.4:c.341C>A	NP_004150.1:p.Ser114Tyr
NM_148919.3:c.353C>A	NP_683720.2:p.Ser118Tyr
NM_148919.4:c.353C>A MANE Select	NP_683720.2:p.Ser118Tyr
NM_004159.5:c.341C>A	NP_004150.1:p.Ser114Tyr