Canonical Allele Identifier: CA2607135
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs780707497
ExAC: 3:129249690 GT / G
gnomAD v2: 3-129249690-GT-G
gnomAD v4: 3-129530847-GT-G
MyVariant Identifiers: chr3:g.129249691del (hg19) chr3:g.129530848del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530848del , CM000665.2:g.129530848del GRCh38
NC_000003.11:g.129249691del , CM000665.1:g.129249691del GRCh37
NC_000003.10:g.130732381del NCBI36
NG_009115.1:g.7210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-28del MANE Select ENSP00000296271.3:n.362-28del
ENST00000296271.3:c.362-28del ENSP00000296271.3:n.362-28del
NM_000539.3:c.362-28del MANE Select NP_000530.1:n.362-28del
Search 100 bp 5'
Search 100 bp 3'