Canonical Allele Identifier: CA363589146

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810488T>G (hg19) ; chr6:g.32842711T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842711T>G , CM000668.2:g.32842711T>G	GRCh38
NC_000006.11:g.32810488T>G , CM000668.1:g.32810488T>G	GRCh37
NC_000006.10:g.32918466T>G	NCBI36
NG_009793.3:g.1060A>C
NG_028165.1:g.7225A>C
NG_009793.4:g.1060A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.547A>C
ENST00000697612.1:n.1225A>C
ENST00000374881.3:c.356A>C	ENSP00000364015.2:p.Asp119Ala
ENST00000374882.8:c.368A>C MANE Select	ENSP00000364016.4:p.Asp123Ala
ENST00000650411.1:n.1689A>C
ENST00000650793.1:n.547A>C
ENST00000374881.2:c.356A>C	ENSP00000364015.2:p.Asp119Ala
ENST00000374882.7:c.368A>C	ENSP00000364016.3:p.Asp123Ala
ENST00000395339.7:c.296A>C	ENSP00000378748.3:p.Asn99Thr
ENST00000484003.1:n.752A>C
NM_004159.4:c.356A>C	NP_004150.1:p.Asp119Ala
NM_148919.3:c.368A>C	NP_683720.2:p.Asp123Ala
NM_148919.4:c.368A>C MANE Select	NP_683720.2:p.Asp123Ala
NM_004159.5:c.356A>C	NP_004150.1:p.Asp119Ala