Canonical Allele Identifier: CA449832898

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810819A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843042A>G , CM000668.2:g.32843042A>G	GRCh38
NC_000006.11:g.32810819A>G , CM000668.1:g.32810819A>G	GRCh37
NC_000006.10:g.32918797A>G	NCBI36
NG_009793.3:g.729T>C
NG_028165.1:g.6894T>C
NG_009793.4:g.729T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.216T>C
ENST00000697612.1:n.894T>C
ENST00000374881.3:c.183T>C	ENSP00000364015.2:p.Val61=
ENST00000374882.8:c.195T>C MANE Select	ENSP00000364016.4:p.Val65=
ENST00000650411.1:n.1516T>C
ENST00000650793.1:n.216T>C
ENST00000374881.2:c.183T>C	ENSP00000364015.2:p.Val61=
ENST00000374882.7:c.195T>C	ENSP00000364016.3:p.Val65=
ENST00000395339.7:c.195T>C	ENSP00000378748.3:p.Val65=
ENST00000484003.1:n.421T>C
NM_004159.4:c.183T>C	NP_004150.1:p.Val61=
NM_148919.3:c.195T>C	NP_683720.2:p.Val65=
NM_148919.4:c.195T>C MANE Select	NP_683720.2:p.Val65=
NM_004159.5:c.183T>C	NP_004150.1:p.Val61=