Canonical Allele Identifier: CA363589117

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810477A>G (hg19) ; chr6:g.32842700A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842700A>G , CM000668.2:g.32842700A>G	GRCh38
NC_000006.11:g.32810477A>G , CM000668.1:g.32810477A>G	GRCh37
NC_000006.10:g.32918455A>G	NCBI36
NG_009793.3:g.1071T>C
NG_028165.1:g.7236T>C
NG_009793.4:g.1071T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.558T>C
ENST00000697612.1:n.1236T>C
ENST00000374881.3:c.367T>C	ENSP00000364015.2:p.Trp123Arg
ENST00000374882.8:c.379T>C MANE Select	ENSP00000364016.4:p.Trp127Arg
ENST00000650411.1:n.1700T>C
ENST00000650793.1:n.558T>C
ENST00000374881.2:c.367T>C	ENSP00000364015.2:p.Trp123Arg
ENST00000374882.7:c.379T>C	ENSP00000364016.3:p.Trp127Arg
ENST00000395339.7:c.307T>C	ENSP00000378748.3:p.Trp103Arg
ENST00000484003.1:n.763T>C
NM_004159.4:c.367T>C	NP_004150.1:p.Trp123Arg
NM_148919.3:c.379T>C	NP_683720.2:p.Trp127Arg
NM_148919.4:c.379T>C MANE Select	NP_683720.2:p.Trp127Arg
NM_004159.5:c.367T>C	NP_004150.1:p.Trp123Arg