Canonical Allele Identifier: CA1401206364
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529125G= , CM000665.2:g.129529125G= GRCh38
NC_000003.11:g.129247968G= , CM000665.1:g.129247968G= GRCh37
NC_000003.10:g.130730658G= NCBI36
NG_009115.1:g.5487G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+31G= MANE Select ENSP00000296271.3:n.361+31G=
ENST00000296271.3:c.361+31G= ENSP00000296271.3:n.361+31G=
NM_000539.3:c.361+31G= MANE Select NP_000530.1:n.361+31G=