Canonical Allele Identifier: CA658821575
Gene: RMRP HGNC NCBI

Linked Data

ClinVar Variation Id: 553820
ClinVar RCV Id: RCV000669342
dbSNP Id: rs1554651106

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657778_35657783del , CM000671.2:g.35657778_35657783del GRCh38
NC_000009.11:g.35657775_35657780del , CM000671.1:g.35657775_35657780del GRCh37
NC_000009.10:g.35647775_35647780del NCBI36
NG_017041.1:g.5238_5243del , LRG_163:g.5238_5243del
NG_033120.1:g.4489_4494del

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.238_243del , LRG_163t1:n.238_243del