Canonical Allele Identifier: CA1401206684
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529283G= , CM000665.2:g.129529283G= GRCh38
NC_000003.11:g.129248126G= , CM000665.1:g.129248126G= GRCh37
NC_000003.10:g.130730816G= NCBI36
NG_009115.1:g.5645G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+189G= MANE Select ENSP00000296271.3:n.361+189G=
ENST00000296271.3:c.361+189G= ENSP00000296271.3:n.361+189G=
NM_000539.3:c.361+189G= MANE Select NP_000530.1:n.361+189G=