Canonical Allele Identifier: CA363589354

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842962-G-A
• MyVariant Identifiers: chr6:g.32810739G>A (hg19) ; chr6:g.32842962G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842962G>A , CM000668.2:g.32842962G>A	GRCh38
NC_000006.11:g.32810739G>A , CM000668.1:g.32810739G>A	GRCh37
NC_000006.10:g.32918717G>A	NCBI36
NG_009793.3:g.809C>T
NG_028165.1:g.6974C>T
NG_009793.4:g.809C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.296C>T
ENST00000697612.1:n.974C>T
ENST00000374881.3:c.263C>T	ENSP00000364015.2:p.Ala88Val
ENST00000374882.8:c.275C>T MANE Select	ENSP00000364016.4:p.Ala92Val
ENST00000650411.1:n.1596C>T
ENST00000650793.1:n.296C>T
ENST00000374881.2:c.263C>T	ENSP00000364015.2:p.Ala88Val
ENST00000374882.7:c.275C>T	ENSP00000364016.3:p.Ala92Val
ENST00000395339.7:c.275C>T	ENSP00000378748.3:p.Ala92Val
ENST00000484003.1:n.501C>T
NM_004159.4:c.263C>T	NP_004150.1:p.Ala88Val
NM_148919.3:c.275C>T	NP_683720.2:p.Ala92Val
NM_148919.4:c.275C>T MANE Select	NP_683720.2:p.Ala92Val
NM_004159.5:c.263C>T	NP_004150.1:p.Ala88Val