Canonical Allele Identifier: CA363589265

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810542T>A (hg19) ; chr6:g.32842765T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842765T>A , CM000668.2:g.32842765T>A	GRCh38
NC_000006.11:g.32810542T>A , CM000668.1:g.32810542T>A	GRCh37
NC_000006.10:g.32918520T>A	NCBI36
NG_009793.3:g.1006A>T
NG_028165.1:g.7171A>T
NG_009793.4:g.1006A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.493A>T
ENST00000697612.1:n.1171A>T
ENST00000374881.3:c.302A>T	ENSP00000364015.2:p.Lys101Met
ENST00000374882.8:c.314A>T MANE Select	ENSP00000364016.4:p.Lys105Met
ENST00000650411.1:n.1635A>T
ENST00000650793.1:n.493A>T
ENST00000374881.2:c.302A>T	ENSP00000364015.2:p.Lys101Met
ENST00000374882.7:c.314A>T	ENSP00000364016.3:p.Lys105Met
ENST00000395339.7:c.296-54A>T	ENSP00000378748.3:n.296-54A>T
ENST00000484003.1:n.698A>T
NM_004159.4:c.302A>T	NP_004150.1:p.Lys101Met
NM_148919.3:c.314A>T	NP_683720.2:p.Lys105Met
NM_148919.4:c.314A>T MANE Select	NP_683720.2:p.Lys105Met
NM_004159.5:c.302A>T	NP_004150.1:p.Lys101Met