Canonical Allele Identifier: CA363589276

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810546T>C (hg19) ; chr6:g.32842769T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842769T>C , CM000668.2:g.32842769T>C	GRCh38
NC_000006.11:g.32810546T>C , CM000668.1:g.32810546T>C	GRCh37
NC_000006.10:g.32918524T>C	NCBI36
NG_009793.3:g.1002A>G
NG_028165.1:g.7167A>G
NG_009793.4:g.1002A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.489A>G
ENST00000697612.1:n.1167A>G
ENST00000374881.3:c.298A>G	ENSP00000364015.2:p.Asn100Asp
ENST00000374882.8:c.310A>G MANE Select	ENSP00000364016.4:p.Asn104Asp
ENST00000650411.1:n.1631A>G
ENST00000650793.1:n.489A>G
ENST00000374881.2:c.298A>G	ENSP00000364015.2:p.Asn100Asp
ENST00000374882.7:c.310A>G	ENSP00000364016.3:p.Asn104Asp
ENST00000395339.7:c.296-58A>G	ENSP00000378748.3:n.296-58A>G
ENST00000484003.1:n.694A>G
NM_004159.4:c.298A>G	NP_004150.1:p.Asn100Asp
NM_148919.3:c.310A>G	NP_683720.2:p.Asn104Asp
NM_148919.4:c.310A>G MANE Select	NP_683720.2:p.Asn104Asp
NM_004159.5:c.298A>G	NP_004150.1:p.Asn100Asp