Canonical Allele Identifier: CA566697890

Gene: PSMB8

Linked Data

• dbSNP Id: rs1216829634
• gnomAD v2: 6-32810602-T-C
• gnomAD v4: 6-32842825-T-C
• MyVariant Identifiers: chr6:g.32810602T>C (hg19) ; chr6:g.32842825T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842825T>C , CM000668.2:g.32842825T>C	GRCh38
NC_000006.11:g.32810602T>C , CM000668.1:g.32810602T>C	GRCh37
NC_000006.10:g.32918580T>C	NCBI36
NG_009793.3:g.946A>G
NG_028165.1:g.7111A>G
NG_009793.4:g.946A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.433A>G
ENST00000697612.1:n.1111A>G
ENST00000374881.3:c.284-42A>G	ENSP00000364015.2:n.284-42A>G
ENST00000374882.8:c.296-42A>G MANE Select	ENSP00000364016.4:n.296-42A>G
ENST00000650411.1:n.1617-42A>G
ENST00000650793.1:n.433A>G
ENST00000374881.2:c.284-42A>G	ENSP00000364015.2:n.284-42A>G
ENST00000374882.7:c.296-42A>G	ENSP00000364016.3:n.296-42A>G
ENST00000395339.7:c.296-114A>G	ENSP00000378748.3:n.296-114A>G
ENST00000484003.1:n.638A>G
NM_004159.4:c.284-42A>G	NP_004150.1:n.284-42A>G
NM_148919.3:c.296-42A>G	NP_683720.2:n.296-42A>G
NM_148919.4:c.296-42A>G MANE Select	NP_683720.2:n.296-42A>G
NM_004159.5:c.284-42A>G	NP_004150.1:n.284-42A>G