Canonical Allele Identifier: CA2607145
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs774865494

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530878G>A , CM000665.2:g.129530878G>A GRCh38
NC_000003.11:g.129249721G>A , CM000665.1:g.129249721G>A GRCh37
NC_000003.10:g.130732411G>A NCBI36
NG_009115.1:g.7240G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.364G>A MANE Select ENSP00000296271.3:p.Glu122Lys
ENST00000296271.3:c.364G>A ENSP00000296271.3:p.Glu122Lys
NM_000539.3:c.364G>A MANE Select NP_000530.1:p.Glu122Lys