Canonical Allele Identifier: CA363589469

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810796G>C (hg19) ; chr6:g.32843019G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843019G>C , CM000668.2:g.32843019G>C	GRCh38
NC_000006.11:g.32810796G>C , CM000668.1:g.32810796G>C	GRCh37
NC_000006.10:g.32918774G>C	NCBI36
NG_009793.3:g.752C>G
NG_028165.1:g.6917C>G
NG_009793.4:g.752C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.239C>G
ENST00000697612.1:n.917C>G
ENST00000374881.3:c.206C>G	ENSP00000364015.2:p.Thr69Ser
ENST00000374882.8:c.218C>G MANE Select	ENSP00000364016.4:p.Thr73Ser
ENST00000650411.1:n.1539C>G
ENST00000650793.1:n.239C>G
ENST00000374881.2:c.206C>G	ENSP00000364015.2:p.Thr69Ser
ENST00000374882.7:c.218C>G	ENSP00000364016.3:p.Thr73Ser
ENST00000395339.7:c.218C>G	ENSP00000378748.3:p.Thr73Ser
ENST00000484003.1:n.444C>G
NM_004159.4:c.206C>G	NP_004150.1:p.Thr69Ser
NM_148919.3:c.218C>G	NP_683720.2:p.Thr73Ser
NM_148919.4:c.218C>G MANE Select	NP_683720.2:p.Thr73Ser
NM_004159.5:c.206C>G	NP_004150.1:p.Thr69Ser