Canonical Allele Identifier: CA3746474

Gene: PSMB8

Linked Data

• ClinVar Variation Id: 1169215
• ClinVar RCV Id: RCV003761387
• dbSNP Id: rs147016287
• ExAC: 6:32810884 G / A
• gnomAD v2: 6-32810884-G-A
• gnomAD v3: 6-32843107-G-A
• gnomAD v4: 6-32843107-G-A
• MyVariant Identifiers: chr6:g.32810884G>A (hg19) ; chr6:g.32843107G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843107G>A , CM000668.2:g.32843107G>A	GRCh38
NC_000006.11:g.32810884G>A , CM000668.1:g.32810884G>A	GRCh37
NC_000006.10:g.32918862G>A	NCBI36
NG_009793.3:g.664C>T
NG_028165.1:g.6829C>T
NG_009793.4:g.664C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.169-18C>T
ENST00000697612.1:n.829C>T
ENST00000374881.3:c.136-18C>T	ENSP00000364015.2:n.136-18C>T
ENST00000374882.8:c.148-18C>T MANE Select	ENSP00000364016.4:n.148-18C>T
ENST00000650411.1:n.1451C>T
ENST00000650793.1:n.169-18C>T
ENST00000374881.2:c.136-18C>T	ENSP00000364015.2:n.136-18C>T
ENST00000374882.7:c.148-18C>T	ENSP00000364016.3:n.148-18C>T
ENST00000395339.7:c.148-18C>T	ENSP00000378748.3:n.148-18C>T
ENST00000484003.1:n.374-18C>T
NM_004159.4:c.136-18C>T	NP_004150.1:n.136-18C>T
NM_148919.3:c.148-18C>T	NP_683720.2:n.148-18C>T
NM_148919.4:c.148-18C>T MANE Select	NP_683720.2:n.148-18C>T
NM_004159.5:c.136-18C>T	NP_004150.1:n.136-18C>T