Canonical Allele Identifier: CA363589281

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810549C>G (hg19) ; chr6:g.32842772C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842772C>G , CM000668.2:g.32842772C>G	GRCh38
NC_000006.11:g.32810549C>G , CM000668.1:g.32810549C>G	GRCh37
NC_000006.10:g.32918527C>G	NCBI36
NG_009793.3:g.999G>C
NG_028165.1:g.7164G>C
NG_009793.4:g.999G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.486G>C
ENST00000697612.1:n.1164G>C
ENST00000374881.3:c.295G>C	ENSP00000364015.2:p.Val99Leu
ENST00000374882.8:c.307G>C MANE Select	ENSP00000364016.4:p.Val103Leu
ENST00000650411.1:n.1628G>C
ENST00000650793.1:n.486G>C
ENST00000374881.2:c.295G>C	ENSP00000364015.2:p.Val99Leu
ENST00000374882.7:c.307G>C	ENSP00000364016.3:p.Val103Leu
ENST00000395339.7:c.296-61G>C	ENSP00000378748.3:n.296-61G>C
ENST00000484003.1:n.691G>C
NM_004159.4:c.295G>C	NP_004150.1:p.Val99Leu
NM_148919.3:c.307G>C	NP_683720.2:p.Val103Leu
NM_148919.4:c.307G>C MANE Select	NP_683720.2:p.Val103Leu
NM_004159.5:c.295G>C	NP_004150.1:p.Val99Leu