Canonical Allele Identifier: CA2607146
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs762059468

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530879A>G , CM000665.2:g.129530879A>G GRCh38
NC_000003.11:g.129249722A>G , CM000665.1:g.129249722A>G GRCh37
NC_000003.10:g.130732412A>G NCBI36
NG_009115.1:g.7241A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.365A>G MANE Select ENSP00000296271.3:p.Glu122Gly
ENST00000296271.3:c.365A>G ENSP00000296271.3:p.Glu122Gly
NM_000539.3:c.365A>G MANE Select NP_000530.1:p.Glu122Gly