Canonical Allele Identifier: CA10654515

Gene: NOP10

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)

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