Canonical Allele Identifier: CA2607189
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs763887860

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531069G>A , CM000665.2:g.129531069G>A GRCh38
NC_000003.11:g.129249912G>A , CM000665.1:g.129249912G>A GRCh37
NC_000003.10:g.130732602G>A NCBI36
NG_009115.1:g.7431G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.530+25G>A MANE Select ENSP00000296271.3:n.530+25G>A
ENST00000296271.3:c.530+25G>A ENSP00000296271.3:n.530+25G>A
NM_000539.3:c.530+25G>A MANE Select NP_000530.1:n.530+25G>A