Canonical Allele Identifier: CA363589210

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810518A>G (hg19) ; chr6:g.32842741A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842741A>G , CM000668.2:g.32842741A>G	GRCh38
NC_000006.11:g.32810518A>G , CM000668.1:g.32810518A>G	GRCh37
NC_000006.10:g.32918496A>G	NCBI36
NG_009793.3:g.1030T>C
NG_028165.1:g.7195T>C
NG_009793.4:g.1030T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.517T>C
ENST00000697612.1:n.1195T>C
ENST00000374881.3:c.326T>C	ENSP00000364015.2:p.Leu109Pro
ENST00000374882.8:c.338T>C MANE Select	ENSP00000364016.4:p.Leu113Pro
ENST00000650411.1:n.1659T>C
ENST00000650793.1:n.517T>C
ENST00000374881.2:c.326T>C	ENSP00000364015.2:p.Leu109Pro
ENST00000374882.7:c.338T>C	ENSP00000364016.3:p.Leu113Pro
ENST00000395339.7:c.296-30T>C	ENSP00000378748.3:n.296-30T>C
ENST00000484003.1:n.722T>C
NM_004159.4:c.326T>C	NP_004150.1:p.Leu109Pro
NM_148919.3:c.338T>C	NP_683720.2:p.Leu113Pro
NM_148919.4:c.338T>C MANE Select	NP_683720.2:p.Leu113Pro
NM_004159.5:c.326T>C	NP_004150.1:p.Leu109Pro