Canonical Allele Identifier: CA823986405

Gene: PSMB8

Linked Data

• dbSNP Id: rs1365841684
• gnomAD v3: 6-32842814-G-A
• gnomAD v4: 6-32842814-G-A
• MyVariant Identifiers: chr6:g.32810591G>A (hg19) ; chr6:g.32842814G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842814G>A , CM000668.2:g.32842814G>A	GRCh38
NC_000006.11:g.32810591G>A , CM000668.1:g.32810591G>A	GRCh37
NC_000006.10:g.32918569G>A	NCBI36
NG_009793.3:g.957C>T
NG_028165.1:g.7122C>T
NG_009793.4:g.957C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.444C>T
ENST00000697612.1:n.1122C>T
ENST00000374881.3:c.284-31C>T	ENSP00000364015.2:n.284-31C>T
ENST00000374882.8:c.296-31C>T MANE Select	ENSP00000364016.4:n.296-31C>T
ENST00000650411.1:n.1617-31C>T
ENST00000650793.1:n.444C>T
ENST00000374881.2:c.284-31C>T	ENSP00000364015.2:n.284-31C>T
ENST00000374882.7:c.296-31C>T	ENSP00000364016.3:n.296-31C>T
ENST00000395339.7:c.296-103C>T	ENSP00000378748.3:n.296-103C>T
ENST00000484003.1:n.649C>T
NM_004159.4:c.284-31C>T	NP_004150.1:n.284-31C>T
NM_148919.3:c.296-31C>T	NP_683720.2:n.296-31C>T
NM_148919.4:c.296-31C>T MANE Select	NP_683720.2:n.296-31C>T
NM_004159.5:c.284-31C>T	NP_004150.1:n.284-31C>T