Canonical Allele Identifier: CA10654515
Gene: NOP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 369090
ClinVar RCV Id: RCV000352550 RCV001675890 RCV003488577
dbSNP Id: rs2169480
gnomAD v2: 15-34635369-A-G
gnomAD v3: 15-34343168-A-G
gnomAD v4: 15-34343168-A-G
MyVariant Identifiers: chr15:g.34635369A>G (hg19) chr15:g.34343168A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34343168A>G , CM000677.2:g.34343168A>G GRCh38
NC_000015.9:g.34635369A>G , CM000677.1:g.34635369A>G GRCh37
NC_000015.8:g.32422661A>G NCBI36
NG_011562.1:g.4994T>C , LRG_345:g.4994T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000557912.2:c.-95T>C ENSP00000453475.1:n.-95T>C
ENST00000699926.1:c.-95T>C ENSP00000514692.1:n.-95T>C
ENST00000328848.5:c.-95T>C ENSP00000332198.4:n.-95T>C
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