Canonical Allele Identifier: CA389147200
Gene: RNASE3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.21360247T>A (hg19) chr14:g.20892088T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20892088T>A , CM000676.2:g.20892088T>A GRCh38
NC_000014.8:g.21360247T>A , CM000676.1:g.21360247T>A GRCh37
NC_000014.7:g.20430087T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000304639.4:c.402T>A MANE Select ENSP00000302324.3:p.Tyr134Ter
ENST00000304639.3:c.402T>A ENSP00000302324.3:p.Tyr134Ter
NM_002935.2:c.402T>A NP_002926.2:p.Tyr134Ter
XR_110261.2:n.209-16345A>T
XR_110261.3:n.726-16345A>T
NM_002935.3:c.402T>A MANE Select NP_002926.2:p.Tyr134Ter
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