Canonical Allele Identifier: CA1401208169
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530520C= , CM000665.2:g.129530520C= GRCh38
NC_000003.11:g.129249363C= , CM000665.1:g.129249363C= GRCh37
NC_000003.10:g.130732053C= NCBI36
NG_009115.1:g.6882C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-356C= MANE Select ENSP00000296271.3:n.362-356C=
ENST00000296271.3:c.362-356C= ENSP00000296271.3:n.362-356C=
NM_000539.3:c.362-356C= MANE Select NP_000530.1:n.362-356C=