Canonical Allele Identifier: CA587570154
Gene: RMRP HGNC NCBI

Linked Data

ClinVar Variation Id: 1982880
ClinVar RCV Id: RCV002795160
dbSNP Id: rs1401833682
gnomAD v2: 9-35657762-AATGAGCCCC-A
gnomAD v4: 9-35657765-AATGAGCCCC-A
MyVariant Identifiers: chr9:g.35657763_35657771del (hg19) chr9:g.35657766_35657774del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657766_35657774del , CM000671.2:g.35657766_35657774del GRCh38
NC_000009.11:g.35657763_35657771del , CM000671.1:g.35657763_35657771del GRCh37
NC_000009.10:g.35647763_35647771del NCBI36
NG_017041.1:g.5245_5253del , LRG_163:g.5245_5253del
NG_033120.1:g.4477_4485del

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.245_253del , LRG_163t1:n.245_253del
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