Canonical Allele Identifier: CA10603132
Gene: RMRP HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657804T>G , CM000671.2:g.35657804T>G GRCh38
NC_000009.11:g.35657801T>G , CM000671.1:g.35657801T>G GRCh37
NC_000009.10:g.35647801T>G NCBI36
NG_017041.1:g.5215A>C , LRG_163:g.5215A>C
NG_033120.1:g.4515T>G

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.215A>C , LRG_163t1:n.215A>C