Canonical Allele Identifier: CA1401210824
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532240C= , CM000665.2:g.129532240C= GRCh38
NC_000003.11:g.129251083C= , CM000665.1:g.129251083C= GRCh37
NC_000003.10:g.130733773C= NCBI36
NG_009115.1:g.8602C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.531-11C= MANE Select ENSP00000296271.3:n.531-11C=
ENST00000296271.3:c.531-11C= ENSP00000296271.3:n.531-11C=
NM_000539.3:c.531-11C= MANE Select NP_000530.1:n.531-11C=