Canonical Allele Identifier: CA464450282
Gene: RMRP HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.35657773T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657776T>A , CM000671.2:g.35657776T>A GRCh38
NC_000009.11:g.35657773T>A , CM000671.1:g.35657773T>A GRCh37
NC_000009.10:g.35647773T>A NCBI36
NG_017041.1:g.5243A>T , LRG_163:g.5243A>T
NG_033120.1:g.4487T>A

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.243A>T , LRG_163t1:n.243A>T