Canonical Allele Identifier: CA363589555

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810835T>A (hg19) ; chr6:g.32843058T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843058T>A , CM000668.2:g.32843058T>A	GRCh38
NC_000006.11:g.32810835T>A , CM000668.1:g.32810835T>A	GRCh37
NC_000006.10:g.32918813T>A	NCBI36
NG_009793.3:g.713A>T
NG_028165.1:g.6878A>T
NG_009793.4:g.713A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.200A>T
ENST00000697612.1:n.878A>T
ENST00000374881.3:c.167A>T	ENSP00000364015.2:p.Asp56Val
ENST00000374882.8:c.179A>T MANE Select	ENSP00000364016.4:p.Asp60Val
ENST00000650411.1:n.1500A>T
ENST00000650793.1:n.200A>T
ENST00000374881.2:c.167A>T	ENSP00000364015.2:p.Asp56Val
ENST00000374882.7:c.179A>T	ENSP00000364016.3:p.Asp60Val
ENST00000395339.7:c.179A>T	ENSP00000378748.3:p.Asp60Val
ENST00000484003.1:n.405A>T
NM_004159.4:c.167A>T	NP_004150.1:p.Asp56Val
NM_148919.3:c.179A>T	NP_683720.2:p.Asp60Val
NM_148919.4:c.179A>T MANE Select	NP_683720.2:p.Asp60Val
NM_004159.5:c.167A>T	NP_004150.1:p.Asp56Val