Canonical Allele Identifier: CA363589570

Gene: PSMB8

Linked Data

• dbSNP Id: rs1221043396
• gnomAD v2: 6-32810842-C-G
• gnomAD v4: 6-32843065-C-G
• MyVariant Identifiers: chr6:g.32810842C>G (hg19) ; chr6:g.32843065C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843065C>G , CM000668.2:g.32843065C>G	GRCh38
NC_000006.11:g.32810842C>G , CM000668.1:g.32810842C>G	GRCh37
NC_000006.10:g.32918820C>G	NCBI36
NG_009793.3:g.706G>C
NG_028165.1:g.6871G>C
NG_009793.4:g.706G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.193G>C
ENST00000697612.1:n.871G>C
ENST00000374881.3:c.160G>C	ENSP00000364015.2:p.Gly54Arg
ENST00000374882.8:c.172G>C MANE Select	ENSP00000364016.4:p.Gly58Arg
ENST00000650411.1:n.1493G>C
ENST00000650793.1:n.193G>C
ENST00000374881.2:c.160G>C	ENSP00000364015.2:p.Gly54Arg
ENST00000374882.7:c.172G>C	ENSP00000364016.3:p.Gly58Arg
ENST00000395339.7:c.172G>C	ENSP00000378748.3:p.Gly58Arg
ENST00000484003.1:n.398G>C
NM_004159.4:c.160G>C	NP_004150.1:p.Gly54Arg
NM_148919.3:c.172G>C	NP_683720.2:p.Gly58Arg
NM_148919.4:c.172G>C MANE Select	NP_683720.2:p.Gly58Arg
NM_004159.5:c.160G>C	NP_004150.1:p.Gly54Arg