Canonical Allele Identifier: CA2703771009
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084772307

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530569_129530570insCACACACACAC , CM000665.2:g.129530569_129530570insCACACACACAC GRCh38
NC_000003.11:g.129249412_129249413insCACACACACAC , CM000665.1:g.129249412_129249413insCACACACACAC GRCh37
NC_000003.10:g.130732102_130732103insCACACACACAC NCBI36
NG_009115.1:g.6931_6932insCACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-307_362-306insCACACACACAC MANE Select ENSP00000296271.3:n.362-307_362-306insCACACACACAC
ENST00000296271.3:c.362-307_362-306insCACACACACAC ENSP00000296271.3:n.362-307_362-306insCACACACACAC
NM_000539.3:c.362-307_362-306insCACACACACAC MANE Select NP_000530.1:n.362-307_362-306insCACACACACAC