Canonical Allele Identifier: CA449832864

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810804G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843027G>C , CM000668.2:g.32843027G>C	GRCh38
NC_000006.11:g.32810804G>C , CM000668.1:g.32810804G>C	GRCh37
NC_000006.10:g.32918782G>C	NCBI36
NG_009793.3:g.744C>G
NG_028165.1:g.6909C>G
NG_009793.4:g.744C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.231C>G
ENST00000697612.1:n.909C>G
ENST00000374881.3:c.198C>G	ENSP00000364015.2:p.Ala66=
ENST00000374882.8:c.210C>G MANE Select	ENSP00000364016.4:p.Ala70=
ENST00000650411.1:n.1531C>G
ENST00000650793.1:n.231C>G
ENST00000374881.2:c.198C>G	ENSP00000364015.2:p.Ala66=
ENST00000374882.7:c.210C>G	ENSP00000364016.3:p.Ala70=
ENST00000395339.7:c.210C>G	ENSP00000378748.3:p.Ala70=
ENST00000484003.1:n.436C>G
NM_004159.4:c.198C>G	NP_004150.1:p.Ala66=
NM_148919.3:c.210C>G	NP_683720.2:p.Ala70=
NM_148919.4:c.210C>G MANE Select	NP_683720.2:p.Ala70=
NM_004159.5:c.198C>G	NP_004150.1:p.Ala66=