Canonical Allele Identifier: CA2678184404

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842661-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842661G>A , CM000668.2:g.32842661G>A	GRCh38
NC_000006.11:g.32810438G>A , CM000668.1:g.32810438G>A	GRCh37
NC_000006.10:g.32918416G>A	NCBI36
NG_009793.3:g.1110C>T
NG_028165.1:g.7275C>T
NG_009793.4:g.1110C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.597C>T
ENST00000697612.1:n.1264+11C>T
ENST00000374881.3:c.395+11C>T	ENSP00000364015.2:n.395+11C>T
ENST00000374882.8:c.407+11C>T MANE Select	ENSP00000364016.4:n.407+11C>T
ENST00000650411.1:n.1728+11C>T
ENST00000650793.1:n.597C>T
ENST00000374881.2:c.395+11C>T	ENSP00000364015.2:n.395+11C>T
ENST00000374882.7:c.407+11C>T	ENSP00000364016.3:n.407+11C>T
ENST00000395339.7:c.335+11C>T	ENSP00000378748.3:n.335+11C>T
ENST00000484003.1:n.791+11C>T
NM_004159.4:c.395+11C>T	NP_004150.1:n.395+11C>T
NM_148919.3:c.407+11C>T	NP_683720.2:n.407+11C>T
NM_148919.4:c.407+11C>T MANE Select	NP_683720.2:n.407+11C>T
NM_004159.5:c.395+11C>T	NP_004150.1:n.395+11C>T