Canonical Allele Identifier: CA485453902
Gene: RNASE3 HGNC NCBI

Linked Data

dbSNP Id: rs1228210608
gnomAD v2: 14-21360319-C-T
gnomAD v3: 14-20892160-C-T
gnomAD v4: 14-20892160-C-T
MyVariant Identifiers: chr14:g.21360319C>T (hg19) chr14:g.20892160C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20892160C>T , CM000676.2:g.20892160C>T GRCh38
NC_000014.8:g.21360319C>T , CM000676.1:g.21360319C>T GRCh37
NC_000014.7:g.20430159C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000304639.4:c.474C>T MANE Select ENSP00000302324.3:p.Thr158=
ENST00000304639.3:c.474C>T ENSP00000302324.3:p.Thr158=
NM_002935.2:c.474C>T NP_002926.2:p.Thr158=
XR_110261.2:n.209-16417G>A
XR_110261.3:n.726-16417G>A
NM_002935.3:c.474C>T MANE Select NP_002926.2:p.Thr158=
Search 100 bp 5'
Search 100 bp 3'