Canonical Allele Identifier: CA464450275
Gene: RMRP HGNC NCBI

Linked Data

ClinVar Variation Id: 557593
ClinVar RCV Id: RCV000673752
dbSNP Id: rs1260135124
gnomAD v2: 9-35657772-G-A
gnomAD v4: 9-35657775-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657775G>A , CM000671.2:g.35657775G>A GRCh38
NC_000009.11:g.35657772G>A , CM000671.1:g.35657772G>A GRCh37
NC_000009.10:g.35647772G>A NCBI36
NG_017041.1:g.5244C>T , LRG_163:g.5244C>T
NG_033120.1:g.4486G>A

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.244C>T , LRG_163t1:n.244C>T