Canonical Allele Identifier: CA485453785
Gene: RNASE3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.21360250A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20892091A>C , CM000676.2:g.20892091A>C GRCh38
NC_000014.8:g.21360250A>C , CM000676.1:g.21360250A>C GRCh37
NC_000014.7:g.20430090A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000304639.4:c.405A>C MANE Select ENSP00000302324.3:p.Val135=
ENST00000304639.3:c.405A>C ENSP00000302324.3:p.Val135=
NM_002935.2:c.405A>C NP_002926.2:p.Val135=
XR_110261.2:n.209-16348T>G
XR_110261.3:n.726-16348T>G
NM_002935.3:c.405A>C MANE Select NP_002926.2:p.Val135=