Canonical Allele Identifier: CA363589088

Gene: PSMB8

Linked Data

• MyVariant Identifiers: chr6:g.32810462C>G (hg19) ; chr6:g.32842685C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842685C>G , CM000668.2:g.32842685C>G	GRCh38
NC_000006.11:g.32810462C>G , CM000668.1:g.32810462C>G	GRCh37
NC_000006.10:g.32918440C>G	NCBI36
NG_009793.3:g.1086G>C
NG_028165.1:g.7251G>C
NG_009793.4:g.1086G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.573G>C
ENST00000697612.1:n.1251G>C
ENST00000374881.3:c.382G>C	ENSP00000364015.2:p.Ala128Pro
ENST00000374882.8:c.394G>C MANE Select	ENSP00000364016.4:p.Ala132Pro
ENST00000650411.1:n.1715G>C
ENST00000650793.1:n.573G>C
ENST00000374881.2:c.382G>C	ENSP00000364015.2:p.Ala128Pro
ENST00000374882.7:c.394G>C	ENSP00000364016.3:p.Ala132Pro
ENST00000395339.7:c.322G>C	ENSP00000378748.3:p.Ala108Pro
ENST00000484003.1:n.778G>C
NM_004159.4:c.382G>C	NP_004150.1:p.Ala128Pro
NM_148919.3:c.394G>C	NP_683720.2:p.Ala132Pro
NM_148919.4:c.394G>C MANE Select	NP_683720.2:p.Ala132Pro
NM_004159.5:c.382G>C	NP_004150.1:p.Ala128Pro