Canonical Allele Identifier: CA449832716

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810735T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842958T>G , CM000668.2:g.32842958T>G	GRCh38
NC_000006.11:g.32810735T>G , CM000668.1:g.32810735T>G	GRCh37
NC_000006.10:g.32918713T>G	NCBI36
NG_009793.3:g.813A>C
NG_028165.1:g.6978A>C
NG_009793.4:g.813A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.300A>C
ENST00000697612.1:n.978A>C
ENST00000374881.3:c.267A>C	ENSP00000364015.2:p.Ser89=
ENST00000374882.8:c.279A>C MANE Select	ENSP00000364016.4:p.Ser93=
ENST00000650411.1:n.1600A>C
ENST00000650793.1:n.300A>C
ENST00000374881.2:c.267A>C	ENSP00000364015.2:p.Ser89=
ENST00000374882.7:c.279A>C	ENSP00000364016.3:p.Ser93=
ENST00000395339.7:c.279A>C	ENSP00000378748.3:p.Ser93=
ENST00000484003.1:n.505A>C
NM_004159.4:c.267A>C	NP_004150.1:p.Ser89=
NM_148919.3:c.279A>C	NP_683720.2:p.Ser93=
NM_148919.4:c.279A>C MANE Select	NP_683720.2:p.Ser93=
NM_004159.5:c.267A>C	NP_004150.1:p.Ser89=