Canonical Allele Identifier: CA2770555254

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843155G>C , CM000668.2:g.32843155G>C	GRCh38
NC_000006.11:g.32810932G>C , CM000668.1:g.32810932G>C	GRCh37
NC_000006.10:g.32918910G>C	NCBI36
NG_009793.3:g.616C>G
NG_028165.1:g.6781C>G
NG_009793.4:g.616C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.169-66C>G
ENST00000697612.1:n.781C>G
ENST00000374881.3:c.136-66C>G	ENSP00000364015.2:n.136-66C>G
ENST00000374882.8:c.148-66C>G MANE Select	ENSP00000364016.4:n.148-66C>G
ENST00000650411.1:n.1403C>G
ENST00000650793.1:n.169-66C>G
ENST00000374881.2:c.136-66C>G	ENSP00000364015.2:n.136-66C>G
ENST00000374882.7:c.148-66C>G	ENSP00000364016.3:n.148-66C>G
ENST00000395339.7:c.148-66C>G	ENSP00000378748.3:n.148-66C>G
ENST00000484003.1:n.374-66C>G
NM_004159.4:c.136-66C>G	NP_004150.1:n.136-66C>G
NM_148919.3:c.148-66C>G	NP_683720.2:n.148-66C>G
NM_148919.4:c.148-66C>G MANE Select	NP_683720.2:n.148-66C>G
NM_004159.5:c.136-66C>G	NP_004150.1:n.136-66C>G