Canonical Allele Identifier: CA192745664
Gene: RMRP HGNC NCBI

Linked Data

ClinVar Variation Id: 1683459
ClinVar RCV Id: RCV002238724
dbSNP Id: rs902757638
gnomAD v2: 9-35657940-G-A
gnomAD v4: 9-35657943-G-A
MyVariant Identifiers: chr9:g.35657940G>A (hg19) chr9:g.35657943G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657943G>A , CM000671.2:g.35657943G>A GRCh38
NC_000009.11:g.35657940G>A , CM000671.1:g.35657940G>A GRCh37
NC_000009.10:g.35647940G>A NCBI36
NG_017041.1:g.5076C>T , LRG_163:g.5076C>T
NG_033120.1:g.4654G>A

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.76C>T , LRG_163t1:n.76C>T
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