Canonical Allele Identifier: CA464450844
Gene: RMRP HGNC NCBI

Linked Data

gnomAD v4: 9-35657938-C-G
MyVariant Identifiers: chr9:g.35657935C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657938C>G , CM000671.2:g.35657938C>G GRCh38
NC_000009.11:g.35657935C>G , CM000671.1:g.35657935C>G GRCh37
NC_000009.10:g.35647935C>G NCBI36
NG_017041.1:g.5081G>C , LRG_163:g.5081G>C
NG_033120.1:g.4649C>G

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.81G>C , LRG_163t1:n.81G>C