Canonical Allele Identifier: CA898751261
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1273801833
MyVariant Identifiers: chr3:g.129249359_129249360insA (hg19) chr3:g.129530516_129530517insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530517dup , CM000665.2:g.129530517dup GRCh38
NC_000003.11:g.129249360dup , CM000665.1:g.129249360dup GRCh37
NC_000003.10:g.130732050dup NCBI36
NG_009115.1:g.6879dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-359dup MANE Select ENSP00000296271.3:n.362-359dup
ENST00000296271.3:c.362-359dup ENSP00000296271.3:n.362-359dup
NM_000539.3:c.362-359dup MANE Select NP_000530.1:n.362-359dup
Search 100 bp 5'
Search 100 bp 3'