Canonical Allele Identifier: CA1401210503
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531870C= , CM000665.2:g.129531870C= GRCh38
NC_000003.11:g.129250713C= , CM000665.1:g.129250713C= GRCh37
NC_000003.10:g.130733403C= NCBI36
NG_009115.1:g.8232C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-381C= MANE Select ENSP00000296271.3:n.531-381C=
ENST00000296271.3:c.531-381C= ENSP00000296271.3:n.531-381C=
NM_000539.3:c.531-381C= MANE Select NP_000530.1:n.531-381C=
Search 100 bp 5'
Search 100 bp 3'