Canonical Allele Identifier: CA1401209104
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530812_129530813delinsAG , CM000665.2:g.129530812_129530813delinsAG GRCh38
NC_000003.11:g.129249655_129249656delinsAG , CM000665.1:g.129249655_129249656delinsAG GRCh37
NC_000003.10:g.130732345_130732346delinsAG NCBI36
NG_009115.1:g.7174_7175delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-64_362-63delinsAG MANE Select ENSP00000296271.3:n.362-64_362-63delinsAG...
ENST00000296271.3:c.362-64_362-63delinsAG ENSP00000296271.3:n.362-64_362-63delinsAG...
NM_000539.3:c.362-64_362-63delinsAG MANE Select NP_000530.1:n.362-64_362-63delinsAG