Canonical Allele Identifier: CA5045870
Gene: RMRP HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.35658014G>A
GRCh37 chr9:g.35658011G>A
gnomAD v2:
9:35658011 G / A
gnomAD v3:
9:35658014 G / A
gnomAD v4:
chr9-35658014-G-A
Joint Max Group AF 0.00019661 (SAS)
Genomes Max Group AF 0.00006809 (NFE)
Exomes Max Group AF 0.00021157 (SAS)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658014G>A , CM000671.2:g.35658014G>A GRCh38
NC_000009.11:g.35658011G>A , CM000671.1:g.35658011G>A GRCh37
NC_000009.10:g.35648011G>A NCBI36
NG_017041.1:g.5005C>T , LRG_163:g.5005C>T
NG_033120.1:g.4725G>A

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.5C>T , LRG_163t1:n.5C>T
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