Canonical Allele Identifier: CA363589582

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810849C>G (hg19) ; chr6:g.32843072C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843072C>G , CM000668.2:g.32843072C>G	GRCh38
NC_000006.11:g.32810849C>G , CM000668.1:g.32810849C>G	GRCh37
NC_000006.10:g.32918827C>G	NCBI36
NG_009793.3:g.699G>C
NG_028165.1:g.6864G>C
NG_009793.4:g.699G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.186G>C
ENST00000697612.1:n.864G>C
ENST00000374881.3:c.153G>C	ENSP00000364015.2:p.Gln51His
ENST00000374882.8:c.165G>C MANE Select	ENSP00000364016.4:p.Gln55His
ENST00000650411.1:n.1486G>C
ENST00000650793.1:n.186G>C
ENST00000374881.2:c.153G>C	ENSP00000364015.2:p.Gln51His
ENST00000374882.7:c.165G>C	ENSP00000364016.3:p.Gln55His
ENST00000395339.7:c.165G>C	ENSP00000378748.3:p.Gln55His
ENST00000484003.1:n.391G>C
NM_004159.4:c.153G>C	NP_004150.1:p.Gln51His
NM_148919.3:c.165G>C	NP_683720.2:p.Gln55His
NM_148919.4:c.165G>C MANE Select	NP_683720.2:p.Gln55His
NM_004159.5:c.153G>C	NP_004150.1:p.Gln51His