Canonical Allele Identifier: CA1401208093
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530476_129530477delinsTG , CM000665.2:g.129530476_129530477delinsTG GRCh38
NC_000003.11:g.129249319_129249320delinsTG , CM000665.1:g.129249319_129249320delinsTG GRCh37
NC_000003.10:g.130732009_130732010delinsTG NCBI36
NG_009115.1:g.6838_6839delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-400_362-399delinsTG MANE Select ENSP00000296271.3:n.362-400_362-399delinsTG
ENST00000296271.3:c.362-400_362-399delinsTG ENSP00000296271.3:n.362-400_362-399delinsTG
NM_000539.3:c.362-400_362-399delinsTG MANE Select NP_000530.1:n.362-400_362-399delinsTG