Canonical Allele Identifier: CA3746440

Gene: PSMB8

Linked Data

• dbSNP Id: rs773255788
• ExAC: 6:32810702 G / A
• gnomAD v2: 6-32810702-G-A
• gnomAD v4: 6-32842925-G-A
• MyVariant Identifiers: chr6:g.32810702G>A (hg19) ; chr6:g.32842925G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842925G>A , CM000668.2:g.32842925G>A	GRCh38
NC_000006.11:g.32810702G>A , CM000668.1:g.32810702G>A	GRCh37
NC_000006.10:g.32918680G>A	NCBI36
NG_009793.3:g.846C>T
NG_028165.1:g.7011C>T
NG_009793.4:g.846C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.333C>T
ENST00000697612.1:n.1011C>T
ENST00000374881.3:c.283+17C>T	ENSP00000364015.2:n.283+17C>T
ENST00000374882.8:c.295+17C>T MANE Select	ENSP00000364016.4:n.295+17C>T
ENST00000650411.1:n.1616+17C>T
ENST00000650793.1:n.333C>T
ENST00000374881.2:c.283+17C>T	ENSP00000364015.2:n.283+17C>T
ENST00000374882.7:c.295+17C>T	ENSP00000364016.3:n.295+17C>T
ENST00000395339.7:c.295+17C>T	ENSP00000378748.3:n.295+17C>T
ENST00000484003.1:n.538C>T
NM_004159.4:c.283+17C>T	NP_004150.1:n.283+17C>T
NM_148919.3:c.295+17C>T	NP_683720.2:n.295+17C>T
NM_148919.4:c.295+17C>T MANE Select	NP_683720.2:n.295+17C>T
NM_004159.5:c.283+17C>T	NP_004150.1:n.283+17C>T