Canonical Allele Identifier: CA2607184
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs776654836

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531044G>A , CM000665.2:g.129531044G>A GRCh38
NC_000003.11:g.129249887G>A , CM000665.1:g.129249887G>A GRCh37
NC_000003.10:g.130732577G>A NCBI36
NG_009115.1:g.7406G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.530G>A MANE Select ENSP00000296271.3:p.Arg177Lys
ENST00000296271.3:c.530G>A ENSP00000296271.3:p.Arg177Lys
NM_000539.3:c.530G>A MANE Select NP_000530.1:p.Arg177Lys