Canonical Allele Identifier: CA464450265
Gene: RMRP HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.35657771C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657774C>A , CM000671.2:g.35657774C>A GRCh38
NC_000009.11:g.35657771C>A , CM000671.1:g.35657771C>A GRCh37
NC_000009.10:g.35647771C>A NCBI36
NG_017041.1:g.5245G>T , LRG_163:g.5245G>T
NG_033120.1:g.4485C>A

Transcript Alleles

HGVS Amino-acid change
NR_003051.3:n.245G>T , LRG_163t1:n.245G>T
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