Canonical Allele Identifier: CA464450859
Gene: RMRP HGNC NCBI

Linked Data

gnomAD v4: 9-35657944-A-T
MyVariant Identifiers: chr9:g.35657941A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657944A>T , CM000671.2:g.35657944A>T GRCh38
NC_000009.11:g.35657941A>T , CM000671.1:g.35657941A>T GRCh37
NC_000009.10:g.35647941A>T NCBI36
NG_017041.1:g.5075T>A , LRG_163:g.5075T>A
NG_033120.1:g.4655A>T

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.75T>A , LRG_163t1:n.75T>A