Canonical Allele Identifier: CA1401209083
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530777T= , CM000665.2:g.129530777T= GRCh38
NC_000003.11:g.129249620T= , CM000665.1:g.129249620T= GRCh37
NC_000003.10:g.130732310T= NCBI36
NG_009115.1:g.7139T=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-99T= MANE Select ENSP00000296271.3:n.362-99T=
ENST00000296271.3:c.362-99T= ENSP00000296271.3:n.362-99T=
NM_000539.3:c.362-99T= MANE Select NP_000530.1:n.362-99T=