Canonical Allele Identifier: CA333053286
Gene: PSMD10 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs111638916

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084839G>A , CM000685.2:g.108084839G>A GRCh38
NC_000023.10:g.107328069G>A , CM000685.1:g.107328069G>A GRCh37
NC_000023.9:g.107214725G>A NCBI36
NG_012521.1:g.11780C>T

Transcript Alleles

HGVS Amino-acid change
NM_002814.3:c.*135C>T VV NP_002805.1:p.=
NM_170750.2:c.*281C>T VV NP_736606.1:p.=
ENST00000217958.7:c.*135C>T ENSP00000217958.3:p.=
ENST00000361815.9:c.*281C>T ENSP00000354906.5:p.=
ENST00000372295.5:c.*135C>T ENSP00000361369.1:p.=
ENST00000372296.5:c.*281C>T ENSP00000361370.1:p.=