Canonical Allele Identifier: CA464450277
Gene: RMRP HGNC NCBI

Linked Data

ClinVar Variation Id: 1386834
ClinVar RCV Id: RCV001875408
dbSNP Id: rs1260135124
gnomAD v2: 9-35657772-G-C
gnomAD v3: 9-35657775-G-C
gnomAD v4: 9-35657775-G-C

Genomic Alleles

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

Transcript Alleles

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