Canonical Allele Identifier: CA464450744
Gene: RMRP HGNC NCBI

Linked Data

dbSNP Id: rs74810894
gnomAD v4: 9-35657891-C-A
MyVariant Identifiers: chr9:g.35657888C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657891C>A , CM000671.2:g.35657891C>A GRCh38
NC_000009.11:g.35657888C>A , CM000671.1:g.35657888C>A GRCh37
NC_000009.10:g.35647888C>A NCBI36
NG_017041.1:g.5128G>T , LRG_163:g.5128G>T
NG_033120.1:g.4602C>A

Transcript Alleles

HGVS Amino-acid change
NR_003051.3:n.128G>T , LRG_163t1:n.128G>T
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