Canonical Allele Identifier: CA464450849
Gene: RMRP HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.35657937G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657940G>T , CM000671.2:g.35657940G>T GRCh38
NC_000009.11:g.35657937G>T , CM000671.1:g.35657937G>T GRCh37
NC_000009.10:g.35647937G>T NCBI36
NG_017041.1:g.5079C>A , LRG_163:g.5079C>A
NG_033120.1:g.4651G>T

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.79C>A , LRG_163t1:n.79C>A
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