Canonical Allele Identifier: CA363589536

Gene: PSMB8

Linked Data

• dbSNP Id: rs1770030436
• MyVariant Identifiers: chr6:g.32810826C>G (hg19) ; chr6:g.32843049C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843049C>G , CM000668.2:g.32843049C>G	GRCh38
NC_000006.11:g.32810826C>G , CM000668.1:g.32810826C>G	GRCh37
NC_000006.10:g.32918804C>G	NCBI36
NG_009793.3:g.722G>C
NG_028165.1:g.6887G>C
NG_009793.4:g.722G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650793.2:n.209G>C
ENST00000697612.1:n.887G>C
ENST00000374881.3:c.176G>C	ENSP00000364015.2:p.Arg59Thr
ENST00000374882.8:c.188G>C MANE Select	ENSP00000364016.4:p.Arg63Thr
ENST00000650411.1:n.1509G>C
ENST00000650793.1:n.209G>C
ENST00000374881.2:c.176G>C	ENSP00000364015.2:p.Arg59Thr
ENST00000374882.7:c.188G>C	ENSP00000364016.3:p.Arg63Thr
ENST00000395339.7:c.188G>C	ENSP00000378748.3:p.Arg63Thr
ENST00000484003.1:n.414G>C
NM_004159.4:c.176G>C	NP_004150.1:p.Arg59Thr
NM_148919.3:c.188G>C	NP_683720.2:p.Arg63Thr
NM_148919.4:c.188G>C MANE Select	NP_683720.2:p.Arg63Thr
NM_004159.5:c.176G>C	NP_004150.1:p.Arg59Thr