Canonical Allele Identifier: CA464450848
Gene: RMRP HGNC NCBI

Linked Data

gnomAD v4: 9-35657940-G-C
MyVariant Identifiers: chr9:g.35657937G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657940G>C , CM000671.2:g.35657940G>C GRCh38
NC_000009.11:g.35657937G>C , CM000671.1:g.35657937G>C GRCh37
NC_000009.10:g.35647937G>C NCBI36
NG_017041.1:g.5079C>G , LRG_163:g.5079C>G
NG_033120.1:g.4651G>C

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.79C>G , LRG_163t1:n.79C>G