Canonical Allele Identifier: CA1401205752
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528973C= , CM000665.2:g.129528973C= GRCh38
NC_000003.11:g.129247816C= , CM000665.1:g.129247816C= GRCh37
NC_000003.10:g.130730506C= NCBI36
NG_009115.1:g.5335C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.240C= MANE Select ENSP00000296271.3:p.Ala80=
ENST00000296271.3:c.240C= ENSP00000296271.3:p.Ala80=
NM_000539.3:c.240C= MANE Select NP_000530.1:p.Ala80=