Canonical Allele Identifier: CA1401205120
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528795G= , CM000665.2:g.129528795G= GRCh38
NC_000003.11:g.129247638G= , CM000665.1:g.129247638G= GRCh37
NC_000003.10:g.130730328G= NCBI36
NG_009115.1:g.5157G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.62G= MANE Select ENSP00000296271.3:p.Arg21=
ENST00000296271.3:c.62G= ENSP00000296271.3:p.Arg21=
NM_000539.3:c.62G= MANE Select NP_000530.1:p.Arg21=