Canonical Allele Identifier: CA137008139

Gene: PSMB8

Linked Data

• dbSNP Id: rs1051889148
• gnomAD v2: 6-32810813-A-C
• gnomAD v4: 6-32843036-A-C
• MyVariant Identifiers: chr6:g.32810813A>C (hg19) ; chr6:g.32843036A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843036A>C , CM000668.2:g.32843036A>C	GRCh38
NC_000006.11:g.32810813A>C , CM000668.1:g.32810813A>C	GRCh37
NC_000006.10:g.32918791A>C	NCBI36
NG_009793.3:g.735T>G
NG_028165.1:g.6900T>G
NG_009793.4:g.735T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.222T>G
ENST00000697612.1:n.900T>G
ENST00000374881.3:c.189T>G	ENSP00000364015.2:p.Ile63Met
ENST00000374882.8:c.201T>G MANE Select	ENSP00000364016.4:p.Ile67Met
ENST00000650411.1:n.1522T>G
ENST00000650793.1:n.222T>G
ENST00000374881.2:c.189T>G	ENSP00000364015.2:p.Ile63Met
ENST00000374882.7:c.201T>G	ENSP00000364016.3:p.Ile67Met
ENST00000395339.7:c.201T>G	ENSP00000378748.3:p.Ile67Met
ENST00000484003.1:n.427T>G
NM_004159.4:c.189T>G	NP_004150.1:p.Ile63Met
NM_148919.3:c.201T>G	NP_683720.2:p.Ile67Met
NM_148919.4:c.201T>G MANE Select	NP_683720.2:p.Ile67Met
NM_004159.5:c.189T>G	NP_004150.1:p.Ile63Met