Canonical Allele Identifier: CA363589163

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810495C>T (hg19) ; chr6:g.32842718C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842718C>T , CM000668.2:g.32842718C>T	GRCh38
NC_000006.11:g.32810495C>T , CM000668.1:g.32810495C>T	GRCh37
NC_000006.10:g.32918473C>T	NCBI36
NG_009793.3:g.1053G>A
NG_028165.1:g.7218G>A
NG_009793.4:g.1053G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.540G>A
ENST00000697612.1:n.1218G>A
ENST00000374881.3:c.349G>A	ENSP00000364015.2:p.Ala117Thr
ENST00000374882.8:c.361G>A MANE Select	ENSP00000364016.4:p.Ala121Thr
ENST00000650411.1:n.1682G>A
ENST00000650793.1:n.540G>A
ENST00000374881.2:c.349G>A	ENSP00000364015.2:p.Ala117Thr
ENST00000374882.7:c.361G>A	ENSP00000364016.3:p.Ala121Thr
ENST00000395339.7:c.296-7G>A	ENSP00000378748.3:n.296-7G>A
ENST00000484003.1:n.745G>A
NM_004159.4:c.349G>A	NP_004150.1:p.Ala117Thr
NM_148919.3:c.361G>A	NP_683720.2:p.Ala121Thr
NM_148919.4:c.361G>A MANE Select	NP_683720.2:p.Ala121Thr
NM_004159.5:c.349G>A	NP_004150.1:p.Ala117Thr