Canonical Allele Identifier: CA363589541

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810828T>G (hg19) ; chr6:g.32843051T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843051T>G , CM000668.2:g.32843051T>G	GRCh38
NC_000006.11:g.32810828T>G , CM000668.1:g.32810828T>G	GRCh37
NC_000006.10:g.32918806T>G	NCBI36
NG_009793.3:g.720A>C
NG_028165.1:g.6885A>C
NG_009793.4:g.720A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650793.2:n.207A>C
ENST00000697612.1:n.885A>C
ENST00000374881.3:c.174A>C	ENSP00000364015.2:p.Glu58Asp
ENST00000374882.8:c.186A>C MANE Select	ENSP00000364016.4:p.Glu62Asp
ENST00000650411.1:n.1507A>C
ENST00000650793.1:n.207A>C
ENST00000374881.2:c.174A>C	ENSP00000364015.2:p.Glu58Asp
ENST00000374882.7:c.186A>C	ENSP00000364016.3:p.Glu62Asp
ENST00000395339.7:c.186A>C	ENSP00000378748.3:p.Glu62Asp
ENST00000484003.1:n.412A>C
NM_004159.4:c.174A>C	NP_004150.1:p.Glu58Asp
NM_148919.3:c.186A>C	NP_683720.2:p.Glu62Asp
NM_148919.4:c.186A>C MANE Select	NP_683720.2:p.Glu62Asp
NM_004159.5:c.174A>C	NP_004150.1:p.Glu58Asp