Canonical Allele Identifier: CA1401211285
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532393C= , CM000665.2:g.129532393C= GRCh38
NC_000003.11:g.129251236C= , CM000665.1:g.129251236C= GRCh37
NC_000003.10:g.130733926C= NCBI36
NG_009115.1:g.8755C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.673C= MANE Select ENSP00000296271.3:p.Gln225=
ENST00000296271.3:c.673C= ENSP00000296271.3:p.Gln225=
NM_000539.3:c.673C= MANE Select NP_000530.1:p.Gln225=