Canonical Allele Identifier: CA363589195

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842733-T-C
• MyVariant Identifiers: chr6:g.32810510T>C (hg19) ; chr6:g.32842733T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842733T>C , CM000668.2:g.32842733T>C	GRCh38
NC_000006.11:g.32810510T>C , CM000668.1:g.32810510T>C	GRCh37
NC_000006.10:g.32918488T>C	NCBI36
NG_009793.3:g.1038A>G
NG_028165.1:g.7203A>G
NG_009793.4:g.1038A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.525A>G
ENST00000697612.1:n.1203A>G
ENST00000374881.3:c.334A>G	ENSP00000364015.2:p.Thr112Ala
ENST00000374882.8:c.346A>G MANE Select	ENSP00000364016.4:p.Thr116Ala
ENST00000650411.1:n.1667A>G
ENST00000650793.1:n.525A>G
ENST00000374881.2:c.334A>G	ENSP00000364015.2:p.Thr112Ala
ENST00000374882.7:c.346A>G	ENSP00000364016.3:p.Thr116Ala
ENST00000395339.7:c.296-22A>G	ENSP00000378748.3:n.296-22A>G
ENST00000484003.1:n.730A>G
NM_004159.4:c.334A>G	NP_004150.1:p.Thr112Ala
NM_148919.3:c.346A>G	NP_683720.2:p.Thr116Ala
NM_148919.4:c.346A>G MANE Select	NP_683720.2:p.Thr116Ala
NM_004159.5:c.334A>G	NP_004150.1:p.Thr112Ala