Canonical Allele Identifier: CA363589297

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810558C>T (hg19) ; chr6:g.32842781C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842781C>T , CM000668.2:g.32842781C>T	GRCh38
NC_000006.11:g.32810558C>T , CM000668.1:g.32810558C>T	GRCh37
NC_000006.10:g.32918536C>T	NCBI36
NG_009793.3:g.990G>A
NG_028165.1:g.7155G>A
NG_009793.4:g.990G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.477G>A
ENST00000697612.1:n.1155G>A
ENST00000374881.3:c.286G>A	ENSP00000364015.2:p.Ala96Thr
ENST00000374882.8:c.298G>A MANE Select	ENSP00000364016.4:p.Ala100Thr
ENST00000650411.1:n.1619G>A
ENST00000650793.1:n.477G>A
ENST00000374881.2:c.286G>A	ENSP00000364015.2:p.Ala96Thr
ENST00000374882.7:c.298G>A	ENSP00000364016.3:p.Ala100Thr
ENST00000395339.7:c.296-70G>A	ENSP00000378748.3:n.296-70G>A
ENST00000484003.1:n.682G>A
NM_004159.4:c.286G>A	NP_004150.1:p.Ala96Thr
NM_148919.3:c.298G>A	NP_683720.2:p.Ala100Thr
NM_148919.4:c.298G>A MANE Select	NP_683720.2:p.Ala100Thr
NM_004159.5:c.286G>A	NP_004150.1:p.Ala96Thr