Canonical Allele Identifier: CA363589258

Gene: PSMB8

Linked Data

• dbSNP Id: rs1769999049
• MyVariant Identifiers: chr6:g.32810539A>G (hg19) ; chr6:g.32842762A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842762A>G , CM000668.2:g.32842762A>G	GRCh38
NC_000006.11:g.32810539A>G , CM000668.1:g.32810539A>G	GRCh37
NC_000006.10:g.32918517A>G	NCBI36
NG_009793.3:g.1009T>C
NG_028165.1:g.7174T>C
NG_009793.4:g.1009T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.496T>C
ENST00000697612.1:n.1174T>C
ENST00000374881.3:c.305T>C	ENSP00000364015.2:p.Val102Ala
ENST00000374882.8:c.317T>C MANE Select	ENSP00000364016.4:p.Val106Ala
ENST00000650411.1:n.1638T>C
ENST00000650793.1:n.496T>C
ENST00000374881.2:c.305T>C	ENSP00000364015.2:p.Val102Ala
ENST00000374882.7:c.317T>C	ENSP00000364016.3:p.Val106Ala
ENST00000395339.7:c.296-51T>C	ENSP00000378748.3:n.296-51T>C
ENST00000484003.1:n.701T>C
NM_004159.4:c.305T>C	NP_004150.1:p.Val102Ala
NM_148919.3:c.317T>C	NP_683720.2:p.Val106Ala
NM_148919.4:c.317T>C MANE Select	NP_683720.2:p.Val106Ala
NM_004159.5:c.305T>C	NP_004150.1:p.Val102Ala