Canonical Allele Identifier: CA898751406
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs60120581
MyVariant Identifiers: chr3:g.129249377_129249388del (hg19) chr3:g.129530534_129530545del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530557_129530568del , CM000665.2:g.129530557_129530568del GRCh38
NC_000003.11:g.129249400_129249411del , CM000665.1:g.129249400_129249411del GRCh37
NC_000003.10:g.130732090_130732101del NCBI36
NG_009115.1:g.6919_6930del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-319_362-308del MANE Select ENSP00000296271.3:n.362-319_362-308del
ENST00000296271.3:c.362-319_362-308del ENSP00000296271.3:n.362-319_362-308del
NM_000539.3:c.362-319_362-308del MANE Select NP_000530.1:n.362-319_362-308del
Search 100 bp 5'
Search 100 bp 3'