Canonical Allele Identifier: CA464450999
Gene: RMRP HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.35657983G>A
GRCh37 chr9:g.35657980G>A
gnomAD v2:
9:35657980 G / A
gnomAD v3:
9:35657983 G / A
gnomAD v4:
chr9-35657983-G-A
Joint Max Group AF 0.00000756 (NFE)
Genomes Max Group AF 0.00000488 (NFE)
Exomes Max Group AF 0.00000562 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657983G>A , CM000671.2:g.35657983G>A GRCh38
NC_000009.11:g.35657980G>A , CM000671.1:g.35657980G>A GRCh37
NC_000009.10:g.35647980G>A NCBI36
NG_017041.1:g.5036C>T , LRG_163:g.5036C>T
NG_033120.1:g.4694G>A

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.36C>T , LRG_163t1:n.36C>T
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