Canonical Allele Identifier: CA3746480

Gene: PSMB8

Linked Data

• dbSNP Id: rs769899420
• ExAC: 6:32810912 G / T
• gnomAD v2: 6-32810912-G-T
• gnomAD v3: 6-32843135-G-T
• gnomAD v4: 6-32843135-G-T
• MyVariant Identifiers: chr6:g.32810912G>T (hg19) ; chr6:g.32843135G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843135G>T , CM000668.2:g.32843135G>T	GRCh38
NC_000006.11:g.32810912G>T , CM000668.1:g.32810912G>T	GRCh37
NC_000006.10:g.32918890G>T	NCBI36
NG_009793.3:g.636C>A
NG_028165.1:g.6801C>A
NG_009793.4:g.636C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.169-46C>A
ENST00000697612.1:n.801C>A
ENST00000374881.3:c.136-46C>A	ENSP00000364015.2:n.136-46C>A
ENST00000374882.8:c.148-46C>A MANE Select	ENSP00000364016.4:n.148-46C>A
ENST00000650411.1:n.1423C>A
ENST00000650793.1:n.169-46C>A
ENST00000374881.2:c.136-46C>A	ENSP00000364015.2:n.136-46C>A
ENST00000374882.7:c.148-46C>A	ENSP00000364016.3:n.148-46C>A
ENST00000395339.7:c.148-46C>A	ENSP00000378748.3:n.148-46C>A
ENST00000484003.1:n.374-46C>A
NM_004159.4:c.136-46C>A	NP_004150.1:n.136-46C>A
NM_148919.3:c.148-46C>A	NP_683720.2:n.148-46C>A
NM_148919.4:c.148-46C>A MANE Select	NP_683720.2:n.148-46C>A
NM_004159.5:c.136-46C>A	NP_004150.1:n.136-46C>A