Canonical Allele Identifier: CA1401212268
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532860G= , CM000665.2:g.129532860G= GRCh38
NC_000003.11:g.129251703G= , CM000665.1:g.129251703G= GRCh37
NC_000003.10:g.130734393G= NCBI36
NG_009115.1:g.9222G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.936+88G= MANE Select ENSP00000296271.3:n.936+88G=
ENST00000296271.3:c.936+88G= ENSP00000296271.3:n.936+88G=
NM_000539.3:c.936+88G= MANE Select NP_000530.1:n.936+88G=