Canonical Allele Identifier: CA1401208197
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084770855

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530525_129530527dup , CM000665.2:g.129530525_129530527dup GRCh38
NC_000003.11:g.129249368_129249370dup , CM000665.1:g.129249368_129249370dup GRCh37
NC_000003.10:g.130732058_130732060dup NCBI36
NG_009115.1:g.6887_6889dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-351_362-349dup MANE Select ENSP00000296271.3:n.362-351_362-349dup
ENST00000296271.3:c.362-351_362-349dup ENSP00000296271.3:n.362-351_362-349dup
NM_000539.3:c.362-351_362-349dup MANE Select NP_000530.1:n.362-351_362-349dup