Canonical Allele Identifier: CA1053435781
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1257173881

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530568_129530569insCACACACAAA , CM000665.2:g.129530568_129530569insCACACACAAA GRCh38
NC_000003.11:g.129249411_129249412insCACACACAAA , CM000665.1:g.129249411_129249412insCACACACAAA GRCh37
NC_000003.10:g.130732101_130732102insCACACACAAA NCBI36
NG_009115.1:g.6930_6931insCACACACAAA

Transcript Alleles

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