Canonical Allele Identifier: CA290479517
Gene: PSMD3 HGNC NCBI

Linked Data

dbSNP Id: rs907749507

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39987219C>G , CM000679.2:g.39987219C>G GRCh38
NC_000017.10:g.38143472C>G , CM000679.1:g.38143472C>G GRCh37
NC_000017.9:g.35396998C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264639.9:c.549+507C>G MANE Select ENSP00000264639.4:n.549+507C>G
ENST00000264639.8:c.549+507C>G ENSP00000264639.4:n.549+507C>G
ENST00000415039.7:c.*23+507C>G ENSP00000407410.3:n.*23+507C>G
ENST00000540504.2:c.104+507C>G
ENST00000580980.1:n.29+507C>G
NM_002809.3:c.549+507C>G NP_002800.2:n.549+507C>G
NM_002809.4:c.549+507C>G MANE Select NP_002800.2:n.549+507C>G