Canonical Allele Identifier: CA363589451

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810784G>T (hg19) ; chr6:g.32843007G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843007G>T , CM000668.2:g.32843007G>T	GRCh38
NC_000006.11:g.32810784G>T , CM000668.1:g.32810784G>T	GRCh37
NC_000006.10:g.32918762G>T	NCBI36
NG_009793.3:g.764C>A
NG_028165.1:g.6929C>A
NG_009793.4:g.764C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.251C>A
ENST00000697612.1:n.929C>A
ENST00000374881.3:c.218C>A	ENSP00000364015.2:p.Ala73Asp
ENST00000374882.8:c.230C>A MANE Select	ENSP00000364016.4:p.Ala77Asp
ENST00000650411.1:n.1551C>A
ENST00000650793.1:n.251C>A
ENST00000374881.2:c.218C>A	ENSP00000364015.2:p.Ala73Asp
ENST00000374882.7:c.230C>A	ENSP00000364016.3:p.Ala77Asp
ENST00000395339.7:c.230C>A	ENSP00000378748.3:p.Ala77Asp
ENST00000484003.1:n.456C>A
NM_004159.4:c.218C>A	NP_004150.1:p.Ala73Asp
NM_148919.3:c.230C>A	NP_683720.2:p.Ala77Asp
NM_148919.4:c.230C>A MANE Select	NP_683720.2:p.Ala77Asp
NM_004159.5:c.218C>A	NP_004150.1:p.Ala73Asp