Canonical Allele Identifier: CA464450915
Gene: RMRP HGNC NCBI

Linked Data

dbSNP Id: rs1187854551
MyVariant Identifiers: chr9:g.35657956G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657959G>C , CM000671.2:g.35657959G>C GRCh38
NC_000009.11:g.35657956G>C , CM000671.1:g.35657956G>C GRCh37
NC_000009.10:g.35647956G>C NCBI36
NG_017041.1:g.5060C>G , LRG_163:g.5060C>G
NG_033120.1:g.4670G>C

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.60C>G , LRG_163t1:n.60C>G