Canonical Allele Identifier: CA464450839
Gene: RMRP HGNC NCBI

Linked Data

ClinVar Variation Id: 968159
ClinVar RCV Id: RCV001243226 RCV001829020
dbSNP Id: rs1372572486
gnomAD v3: 9-35657936-G-C
gnomAD v4: 9-35657936-G-C
MyVariant Identifiers: chr9:g.35657933G>C (hg19) chr9:g.35657936G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657936G>C , CM000671.2:g.35657936G>C GRCh38
NC_000009.11:g.35657933G>C , CM000671.1:g.35657933G>C GRCh37
NC_000009.10:g.35647933G>C NCBI36
NG_017041.1:g.5083C>G , LRG_163:g.5083C>G
NG_033120.1:g.4647G>C

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.83C>G , LRG_163t1:n.83C>G
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