Canonical Allele Identifier: CA1053435638
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084771508

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530534_129530535insAACA , CM000665.2:g.129530534_129530535insAACA GRCh38
NC_000003.11:g.129249377_129249378insAACA , CM000665.1:g.129249377_129249378insAACA GRCh37
NC_000003.10:g.130732067_130732068insAACA NCBI36
NG_009115.1:g.6896_6897insAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-342_362-341insAACA MANE Select ENSP00000296271.3:n.362-342_362-341insAACA
ENST00000296271.3:c.362-342_362-341insAACA ENSP00000296271.3:n.362-342_362-341insAACA
NM_000539.3:c.362-342_362-341insAACA MANE Select NP_000530.1:n.362-342_362-341insAACA