Canonical Allele Identifier: CA192745661
Gene: RMRP HGNC NCBI

Linked Data

dbSNP Id: rs949582348
gnomAD v2: 9-35657937-G-A
gnomAD v3: 9-35657940-G-A
gnomAD v4: 9-35657940-G-A
MyVariant Identifiers: chr9:g.35657937G>A (hg19) chr9:g.35657940G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657940G>A , CM000671.2:g.35657940G>A GRCh38
NC_000009.11:g.35657937G>A , CM000671.1:g.35657937G>A GRCh37
NC_000009.10:g.35647937G>A NCBI36
NG_017041.1:g.5079C>T , LRG_163:g.5079C>T
NG_033120.1:g.4651G>A

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.79C>T , LRG_163t1:n.79C>T
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