Canonical Allele Identifier: CA464451014
Gene: RMRP HGNC NCBI

Linked Data

dbSNP Id: rs1823627300
MyVariant Identifiers: chr9:g.35657986A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657989A>C , CM000671.2:g.35657989A>C GRCh38
NC_000009.11:g.35657986A>C , CM000671.1:g.35657986A>C GRCh37
NC_000009.10:g.35647986A>C NCBI36
NG_017041.1:g.5030T>G , LRG_163:g.5030T>G
NG_033120.1:g.4700A>C

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.30T>G , LRG_163t1:n.30T>G