Canonical Allele Identifier: CA449832597

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810555A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842778A>G , CM000668.2:g.32842778A>G	GRCh38
NC_000006.11:g.32810555A>G , CM000668.1:g.32810555A>G	GRCh37
NC_000006.10:g.32918533A>G	NCBI36
NG_009793.3:g.993T>C
NG_028165.1:g.7158T>C
NG_009793.4:g.993T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.480T>C
ENST00000697612.1:n.1158T>C
ENST00000374881.3:c.289T>C	ENSP00000364015.2:p.Leu97=
ENST00000374882.8:c.301T>C MANE Select	ENSP00000364016.4:p.Leu101=
ENST00000650411.1:n.1622T>C
ENST00000650793.1:n.480T>C
ENST00000374881.2:c.289T>C	ENSP00000364015.2:p.Leu97=
ENST00000374882.7:c.301T>C	ENSP00000364016.3:p.Leu101=
ENST00000395339.7:c.296-67T>C	ENSP00000378748.3:n.296-67T>C
ENST00000484003.1:n.685T>C
NM_004159.4:c.289T>C	NP_004150.1:p.Leu97=
NM_148919.3:c.301T>C	NP_683720.2:p.Leu101=
NM_148919.4:c.301T>C MANE Select	NP_683720.2:p.Leu101=
NM_004159.5:c.289T>C	NP_004150.1:p.Leu97=