Canonical Allele Identifier: CA363589122

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810479T>C (hg19) ; chr6:g.32842702T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842702T>C , CM000668.2:g.32842702T>C	GRCh38
NC_000006.11:g.32810479T>C , CM000668.1:g.32810479T>C	GRCh37
NC_000006.10:g.32918457T>C	NCBI36
NG_009793.3:g.1069A>G
NG_028165.1:g.7234A>G
NG_009793.4:g.1069A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.556A>G
ENST00000697612.1:n.1234A>G
ENST00000374881.3:c.365A>G	ENSP00000364015.2:p.Tyr122Cys
ENST00000374882.8:c.377A>G MANE Select	ENSP00000364016.4:p.Tyr126Cys
ENST00000650411.1:n.1698A>G
ENST00000650793.1:n.556A>G
ENST00000374881.2:c.365A>G	ENSP00000364015.2:p.Tyr122Cys
ENST00000374882.7:c.377A>G	ENSP00000364016.3:p.Tyr126Cys
ENST00000395339.7:c.305A>G	ENSP00000378748.3:p.Tyr102Cys
ENST00000484003.1:n.761A>G
NM_004159.4:c.365A>G	NP_004150.1:p.Tyr122Cys
NM_148919.3:c.377A>G	NP_683720.2:p.Tyr126Cys
NM_148919.4:c.377A>G MANE Select	NP_683720.2:p.Tyr126Cys
NM_004159.5:c.365A>G	NP_004150.1:p.Tyr122Cys