Canonical Allele Identifier: CA464450999

Gene: RMRP

Linked Data

• ClinVar Variation Id: 533761
• ClinVar RCV Id: RCV000641006 ; RCV001273834 ; RCV002499076
• dbSNP Id: rs549085067
• gnomAD v2: 9-35657980-G-A
• gnomAD v3: 9-35657983-G-A
• gnomAD v4: 9-35657983-G-A
• MyVariant Identifiers: chr9:g.35657980G>A (hg19) ; chr9:g.35657983G>A (hg38)

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