Canonical Allele Identifier: CA464450279
Gene: RMRP HGNC NCBI

Linked Data

dbSNP Id: rs1260135124
gnomAD v3: 9-35657775-G-T
gnomAD v4: 9-35657775-G-T
MyVariant Identifiers: chr9:g.35657772G>T (hg19) chr9:g.35657775G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657775G>T , CM000671.2:g.35657775G>T GRCh38
NC_000009.11:g.35657772G>T , CM000671.1:g.35657772G>T GRCh37
NC_000009.10:g.35647772G>T NCBI36
NG_017041.1:g.5244C>A , LRG_163:g.5244C>A
NG_033120.1:g.4486G>T

Transcript Alleles

HGVS Amino-acid change
NR_003051.3:n.244C>A , LRG_163t1:n.244C>A
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