Canonical Allele Identifier: CA2678184396

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842654-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842654A>G , CM000668.2:g.32842654A>G	GRCh38
NC_000006.11:g.32810431A>G , CM000668.1:g.32810431A>G	GRCh37
NC_000006.10:g.32918409A>G	NCBI36
NG_009793.3:g.1117T>C
NG_028165.1:g.7282T>C
NG_009793.4:g.1117T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.604T>C
ENST00000697612.1:n.1264+18T>C
ENST00000374881.3:c.395+18T>C	ENSP00000364015.2:n.395+18T>C
ENST00000374882.8:c.407+18T>C MANE Select	ENSP00000364016.4:n.407+18T>C
ENST00000650411.1:n.1728+18T>C
ENST00000650793.1:n.604T>C
ENST00000374881.2:c.395+18T>C	ENSP00000364015.2:n.395+18T>C
ENST00000374882.7:c.407+18T>C	ENSP00000364016.3:n.407+18T>C
ENST00000395339.7:c.335+18T>C	ENSP00000378748.3:n.335+18T>C
ENST00000484003.1:n.791+18T>C
NM_004159.4:c.395+18T>C	NP_004150.1:n.395+18T>C
NM_148919.3:c.407+18T>C	NP_683720.2:n.407+18T>C
NM_148919.4:c.407+18T>C MANE Select	NP_683720.2:n.407+18T>C
NM_004159.5:c.395+18T>C	NP_004150.1:n.395+18T>C