Canonical Allele Identifier: CA464450258
Gene: RMRP HGNC NCBI

Linked Data

gnomAD v4: 9-35657773-C-A
MyVariant Identifiers: chr9:g.35657770C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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