Canonical Allele Identifier: CA449832596

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810553T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842776T>C , CM000668.2:g.32842776T>C	GRCh38
NC_000006.11:g.32810553T>C , CM000668.1:g.32810553T>C	GRCh37
NC_000006.10:g.32918531T>C	NCBI36
NG_009793.3:g.995A>G
NG_028165.1:g.7160A>G
NG_009793.4:g.995A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.482A>G
ENST00000697612.1:n.1160A>G
ENST00000374881.3:c.291A>G	ENSP00000364015.2:p.Leu97=
ENST00000374882.8:c.303A>G MANE Select	ENSP00000364016.4:p.Leu101=
ENST00000650411.1:n.1624A>G
ENST00000650793.1:n.482A>G
ENST00000374881.2:c.291A>G	ENSP00000364015.2:p.Leu97=
ENST00000374882.7:c.303A>G	ENSP00000364016.3:p.Leu101=
ENST00000395339.7:c.296-65A>G	ENSP00000378748.3:n.296-65A>G
ENST00000484003.1:n.687A>G
NM_004159.4:c.291A>G	NP_004150.1:p.Leu97=
NM_148919.3:c.303A>G	NP_683720.2:p.Leu101=
NM_148919.4:c.303A>G MANE Select	NP_683720.2:p.Leu101=
NM_004159.5:c.291A>G	NP_004150.1:p.Leu97=