Canonical Allele Identifier: CA363589524

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810820A>T (hg19) ; chr6:g.32843043A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843043A>T , CM000668.2:g.32843043A>T	GRCh38
NC_000006.11:g.32810820A>T , CM000668.1:g.32810820A>T	GRCh37
NC_000006.10:g.32918798A>T	NCBI36
NG_009793.3:g.728T>A
NG_028165.1:g.6893T>A
NG_009793.4:g.728T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.215T>A
ENST00000697612.1:n.893T>A
ENST00000374881.3:c.182T>A	ENSP00000364015.2:p.Val61Asp
ENST00000374882.8:c.194T>A MANE Select	ENSP00000364016.4:p.Val65Asp
ENST00000650411.1:n.1515T>A
ENST00000650793.1:n.215T>A
ENST00000374881.2:c.182T>A	ENSP00000364015.2:p.Val61Asp
ENST00000374882.7:c.194T>A	ENSP00000364016.3:p.Val65Asp
ENST00000395339.7:c.194T>A	ENSP00000378748.3:p.Val65Asp
ENST00000484003.1:n.420T>A
NM_004159.4:c.182T>A	NP_004150.1:p.Val61Asp
NM_148919.3:c.194T>A	NP_683720.2:p.Val65Asp
NM_148919.4:c.194T>A MANE Select	NP_683720.2:p.Val65Asp
NM_004159.5:c.182T>A	NP_004150.1:p.Val61Asp