Canonical Allele Identifier: CA1401210855
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532256_129532257delinsTC , CM000665.2:g.129532256_129532257delinsTC GRCh38
NC_000003.11:g.129251099_129251100delinsTC , CM000665.1:g.129251099_129251100delinsTC GRCh37
NC_000003.10:g.130733789_130733790delinsTC NCBI36
NG_009115.1:g.8618_8619delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.536_537delinsTC MANE Select ENSP00000296271.3:p.Ile179=
ENST00000296271.3:c.536_537delinsTC ENSP00000296271.3:p.Ile179=
NM_000539.3:c.536_537delinsTC MANE Select NP_000530.1:p.Ile179=