Canonical Allele Identifier: CA2578579578

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842831C>A , CM000668.2:g.32842831C>A	GRCh38
NC_000006.11:g.32810608C>A , CM000668.1:g.32810608C>A	GRCh37
NC_000006.10:g.32918586C>A	NCBI36
NG_009793.3:g.940G>T
NG_028165.1:g.7105G>T
NG_009793.4:g.940G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.427G>T
ENST00000697612.1:n.1105G>T
ENST00000374881.3:c.284-48G>T	ENSP00000364015.2:n.284-48G>T
ENST00000374882.8:c.296-48G>T MANE Select	ENSP00000364016.4:n.296-48G>T
ENST00000650411.1:n.1617-48G>T
ENST00000650793.1:n.427G>T
ENST00000374881.2:c.284-48G>T	ENSP00000364015.2:n.284-48G>T
ENST00000374882.7:c.296-48G>T	ENSP00000364016.3:n.296-48G>T
ENST00000395339.7:c.295+111G>T	ENSP00000378748.3:n.295+111G>T
ENST00000484003.1:n.632G>T
NM_004159.4:c.284-48G>T	NP_004150.1:n.284-48G>T
NM_148919.3:c.296-48G>T	NP_683720.2:n.296-48G>T
NM_148919.4:c.296-48G>T MANE Select	NP_683720.2:n.296-48G>T
NM_004159.5:c.284-48G>T	NP_004150.1:n.284-48G>T