Canonical Allele Identifier: CA464450260
Gene: RMRP HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.35657770C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657773C>G , CM000671.2:g.35657773C>G GRCh38
NC_000009.11:g.35657770C>G , CM000671.1:g.35657770C>G GRCh37
NC_000009.10:g.35647770C>G NCBI36
NG_017041.1:g.5246G>C , LRG_163:g.5246G>C
NG_033120.1:g.4484C>G

Transcript Alleles

HGVS Amino-acid change
NR_003051.3:n.246G>C , LRG_163t1:n.246G>C