Canonical Allele Identifier: CA1401210709
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532154G= , CM000665.2:g.129532154G= GRCh38
NC_000003.11:g.129250997G= , CM000665.1:g.129250997G= GRCh37
NC_000003.10:g.130733687G= NCBI36
NG_009115.1:g.8516G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.531-97G= MANE Select ENSP00000296271.3:n.531-97G=
ENST00000296271.3:c.531-97G= ENSP00000296271.3:n.531-97G=
NM_000539.3:c.531-97G= MANE Select NP_000530.1:n.531-97G=