Canonical Allele Identifier: CA363589059

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842673-T-C
• MyVariant Identifiers: chr6:g.32810450T>C (hg19) ; chr6:g.32842673T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842673T>C , CM000668.2:g.32842673T>C	GRCh38
NC_000006.11:g.32810450T>C , CM000668.1:g.32810450T>C	GRCh37
NC_000006.10:g.32918428T>C	NCBI36
NG_009793.3:g.1098A>G
NG_028165.1:g.7263A>G
NG_009793.4:g.1098A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.585A>G
ENST00000697612.1:n.1263A>G
ENST00000374881.3:c.394A>G	ENSP00000364015.2:p.Arg132Gly
ENST00000374882.8:c.406A>G MANE Select	ENSP00000364016.4:p.Arg136Gly
ENST00000650411.1:n.1727A>G
ENST00000650793.1:n.585A>G
ENST00000374881.2:c.394A>G	ENSP00000364015.2:p.Arg132Gly
ENST00000374882.7:c.406A>G	ENSP00000364016.3:p.Arg136Gly
ENST00000395339.7:c.334A>G	ENSP00000378748.3:p.Arg112Gly
ENST00000484003.1:n.790A>G
NM_004159.4:c.394A>G	NP_004150.1:p.Arg132Gly
NM_148919.3:c.406A>G	NP_683720.2:p.Arg136Gly
NM_148919.4:c.406A>G MANE Select	NP_683720.2:p.Arg136Gly
NM_004159.5:c.394A>G	NP_004150.1:p.Arg132Gly