Canonical Allele Identifier: CA363589138

Gene: PSMB8

Linked Data

• dbSNP Id: rs767636318
• gnomAD v3: 6-32842708-C-T
• gnomAD v4: 6-32842708-C-T
• MyVariant Identifiers: chr6:g.32810485C>T (hg19) ; chr6:g.32842708C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842708C>T , CM000668.2:g.32842708C>T	GRCh38
NC_000006.11:g.32810485C>T , CM000668.1:g.32810485C>T	GRCh37
NC_000006.10:g.32918463C>T	NCBI36
NG_009793.3:g.1063G>A
NG_028165.1:g.7228G>A
NG_009793.4:g.1063G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.550G>A
ENST00000697612.1:n.1228G>A
ENST00000374881.3:c.359G>A	ENSP00000364015.2:p.Cys120Tyr
ENST00000374882.8:c.371G>A MANE Select	ENSP00000364016.4:p.Cys124Tyr
ENST00000650411.1:n.1692G>A
ENST00000650793.1:n.550G>A
ENST00000374881.2:c.359G>A	ENSP00000364015.2:p.Cys120Tyr
ENST00000374882.7:c.371G>A	ENSP00000364016.3:p.Cys124Tyr
ENST00000395339.7:c.299G>A	ENSP00000378748.3:p.Cys100Tyr
ENST00000484003.1:n.755G>A
NM_004159.4:c.359G>A	NP_004150.1:p.Cys120Tyr
NM_148919.3:c.371G>A	NP_683720.2:p.Cys124Tyr
NM_148919.4:c.371G>A MANE Select	NP_683720.2:p.Cys124Tyr
NM_004159.5:c.359G>A	NP_004150.1:p.Cys120Tyr