Canonical Allele Identifier: CA2678184935

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32843150-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843150A>G , CM000668.2:g.32843150A>G	GRCh38
NC_000006.11:g.32810927A>G , CM000668.1:g.32810927A>G	GRCh37
NC_000006.10:g.32918905A>G	NCBI36
NG_009793.3:g.621T>C
NG_028165.1:g.6786T>C
NG_009793.4:g.621T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.169-61T>C
ENST00000697612.1:n.786T>C
ENST00000374881.3:c.136-61T>C	ENSP00000364015.2:n.136-61T>C
ENST00000374882.8:c.148-61T>C MANE Select	ENSP00000364016.4:n.148-61T>C
ENST00000650411.1:n.1408T>C
ENST00000650793.1:n.169-61T>C
ENST00000374881.2:c.136-61T>C	ENSP00000364015.2:n.136-61T>C
ENST00000374882.7:c.148-61T>C	ENSP00000364016.3:n.148-61T>C
ENST00000395339.7:c.148-61T>C	ENSP00000378748.3:n.148-61T>C
ENST00000484003.1:n.374-61T>C
NM_004159.4:c.136-61T>C	NP_004150.1:n.136-61T>C
NM_148919.3:c.148-61T>C	NP_683720.2:n.148-61T>C
NM_148919.4:c.148-61T>C MANE Select	NP_683720.2:n.148-61T>C
NM_004159.5:c.136-61T>C	NP_004150.1:n.136-61T>C