Canonical Allele Identifier: CA363589533

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810824T>C (hg19) ; chr6:g.32843047T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843047T>C , CM000668.2:g.32843047T>C	GRCh38
NC_000006.11:g.32810824T>C , CM000668.1:g.32810824T>C	GRCh37
NC_000006.10:g.32918802T>C	NCBI36
NG_009793.3:g.724A>G
NG_028165.1:g.6889A>G
NG_009793.4:g.724A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650793.2:n.211A>G
ENST00000697612.1:n.889A>G
ENST00000374881.3:c.178A>G	ENSP00000364015.2:p.Asn60Asp
ENST00000374882.8:c.190A>G MANE Select	ENSP00000364016.4:p.Asn64Asp
ENST00000650411.1:n.1511A>G
ENST00000650793.1:n.211A>G
ENST00000374881.2:c.178A>G	ENSP00000364015.2:p.Asn60Asp
ENST00000374882.7:c.190A>G	ENSP00000364016.3:p.Asn64Asp
ENST00000395339.7:c.190A>G	ENSP00000378748.3:p.Asn64Asp
ENST00000484003.1:n.416A>G
NM_004159.4:c.178A>G	NP_004150.1:p.Asn60Asp
NM_148919.3:c.190A>G	NP_683720.2:p.Asn64Asp
NM_148919.4:c.190A>G MANE Select	NP_683720.2:p.Asn64Asp
NM_004159.5:c.178A>G	NP_004150.1:p.Asn60Asp