Canonical Allele Identifier: CA363589548

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810832C>A (hg19) ; chr6:g.32843055C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843055C>A , CM000668.2:g.32843055C>A	GRCh38
NC_000006.11:g.32810832C>A , CM000668.1:g.32810832C>A	GRCh37
NC_000006.10:g.32918810C>A	NCBI36
NG_009793.3:g.716G>T
NG_028165.1:g.6881G>T
NG_009793.4:g.716G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650793.2:n.203G>T
ENST00000697612.1:n.881G>T
ENST00000374881.3:c.170G>T	ENSP00000364015.2:p.Gly57Val
ENST00000374882.8:c.182G>T MANE Select	ENSP00000364016.4:p.Gly61Val
ENST00000650411.1:n.1503G>T
ENST00000650793.1:n.203G>T
ENST00000374881.2:c.170G>T	ENSP00000364015.2:p.Gly57Val
ENST00000374882.7:c.182G>T	ENSP00000364016.3:p.Gly61Val
ENST00000395339.7:c.182G>T	ENSP00000378748.3:p.Gly61Val
ENST00000484003.1:n.408G>T
NM_004159.4:c.170G>T	NP_004150.1:p.Gly57Val
NM_148919.3:c.182G>T	NP_683720.2:p.Gly61Val
NM_148919.4:c.182G>T MANE Select	NP_683720.2:p.Gly61Val
NM_004159.5:c.170G>T	NP_004150.1:p.Gly57Val