Canonical Allele Identifier: CA363589135

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810484A>C (hg19) ; chr6:g.32842707A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842707A>C , CM000668.2:g.32842707A>C	GRCh38
NC_000006.11:g.32810484A>C , CM000668.1:g.32810484A>C	GRCh37
NC_000006.10:g.32918462A>C	NCBI36
NG_009793.3:g.1064T>G
NG_028165.1:g.7229T>G
NG_009793.4:g.1064T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.551T>G
ENST00000697612.1:n.1229T>G
ENST00000374881.3:c.360T>G	ENSP00000364015.2:p.Cys120Trp
ENST00000374882.8:c.372T>G MANE Select	ENSP00000364016.4:p.Cys124Trp
ENST00000650411.1:n.1693T>G
ENST00000650793.1:n.551T>G
ENST00000374881.2:c.360T>G	ENSP00000364015.2:p.Cys120Trp
ENST00000374882.7:c.372T>G	ENSP00000364016.3:p.Cys124Trp
ENST00000395339.7:c.300T>G	ENSP00000378748.3:p.Cys100Trp
ENST00000484003.1:n.756T>G
NM_004159.4:c.360T>G	NP_004150.1:p.Cys120Trp
NM_148919.3:c.372T>G	NP_683720.2:p.Cys124Trp
NM_148919.4:c.372T>G MANE Select	NP_683720.2:p.Cys124Trp
NM_004159.5:c.360T>G	NP_004150.1:p.Cys120Trp