Canonical Allele Identifier: CA1401210765
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532210A= , CM000665.2:g.129532210A= GRCh38
NC_000003.11:g.129251053A= , CM000665.1:g.129251053A= GRCh37
NC_000003.10:g.130733743A= NCBI36
NG_009115.1:g.8572A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-41A= MANE Select ENSP00000296271.3:n.531-41A=
ENST00000296271.3:c.531-41A= ENSP00000296271.3:n.531-41A=
NM_000539.3:c.531-41A= MANE Select NP_000530.1:n.531-41A=