Canonical Allele Identifier: CA363589356

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810739G>T (hg19) ; chr6:g.32842962G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842962G>T , CM000668.2:g.32842962G>T	GRCh38
NC_000006.11:g.32810739G>T , CM000668.1:g.32810739G>T	GRCh37
NC_000006.10:g.32918717G>T	NCBI36
NG_009793.3:g.809C>A
NG_028165.1:g.6974C>A
NG_009793.4:g.809C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.296C>A
ENST00000697612.1:n.974C>A
ENST00000374881.3:c.263C>A	ENSP00000364015.2:p.Ala88Asp
ENST00000374882.8:c.275C>A MANE Select	ENSP00000364016.4:p.Ala92Asp
ENST00000650411.1:n.1596C>A
ENST00000650793.1:n.296C>A
ENST00000374881.2:c.263C>A	ENSP00000364015.2:p.Ala88Asp
ENST00000374882.7:c.275C>A	ENSP00000364016.3:p.Ala92Asp
ENST00000395339.7:c.275C>A	ENSP00000378748.3:p.Ala92Asp
ENST00000484003.1:n.501C>A
NM_004159.4:c.263C>A	NP_004150.1:p.Ala88Asp
NM_148919.3:c.275C>A	NP_683720.2:p.Ala92Asp
NM_148919.4:c.275C>A MANE Select	NP_683720.2:p.Ala92Asp
NM_004159.5:c.263C>A	NP_004150.1:p.Ala88Asp