Canonical Allele Identifier: CA1401208880
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084772094

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530568_129530569insCACACACAGACACA , CM000665.2:g.129530568_129530569insCACACACAGACACA GRCh38
NC_000003.11:g.129249411_129249412insCACACACAGACACA , CM000665.1:g.129249411_129249412insCACACACAGACACA GRCh37
NC_000003.10:g.130732101_130732102insCACACACAGACACA NCBI36
NG_009115.1:g.6930_6931insCACACACAGACACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-308_362-307insCACACACAGACACA MANE Select ENSP00000296271.3:n.362-308_362-307insCACACACAGACACA
ENST00000296271.3:c.362-308_362-307insCACACACAGACACA ENSP00000296271.3:n.362-308_362-307insCACACACAGACACA
NM_000539.3:c.362-308_362-307insCACACACAGACACA MANE Select NP_000530.1:n.362-308_362-307insCACACACAGACACA