Canonical Allele Identifier: CA464450835
Gene: RMRP HGNC NCBI

Linked Data

ClinVar Variation Id: 1417612
ClinVar RCV Id: RCV001938501
dbSNP Id: rs1282617590
gnomAD v3: 9-35657935-G-A
gnomAD v4: 9-35657935-G-A
MyVariant Identifiers: chr9:g.35657932G>A (hg19) chr9:g.35657935G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657935G>A , CM000671.2:g.35657935G>A GRCh38
NC_000009.11:g.35657932G>A , CM000671.1:g.35657932G>A GRCh37
NC_000009.10:g.35647932G>A NCBI36
NG_017041.1:g.5084C>T , LRG_163:g.5084C>T
NG_033120.1:g.4646G>A

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.84C>T , LRG_163t1:n.84C>T
Search 100 bp 5'
Search 100 bp 3'