Canonical Allele Identifier: CA333053203
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs1028570002
MyVariant Identifiers: chrX:g.107327628T>C (hg19) chrX:g.108084398T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084398T>C , CM000685.2:g.108084398T>C GRCh38
NC_000023.10:g.107327628T>C , CM000685.1:g.107327628T>C GRCh37
NC_000023.9:g.107214284T>C NCBI36
NG_012521.1:g.12221A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*576A>G MANE Select ENSP00000217958.3:n.*576A>G
ENST00000217958.7:c.*576A>G ENSP00000217958.3:n.*576A>G
NM_002814.3:c.*576A>G NP_002805.1:n.*576A>G
NM_170750.2:c.*722A>G NP_736606.1:n.*722A>G
NM_002814.4:c.*576A>G MANE Select NP_002805.1:n.*576A>G
NM_170750.3:c.*722A>G NP_736606.1:n.*722A>G
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