Canonical Allele Identifier: CA354496869
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 802005
ClinVar RCV Id: RCV000987329
dbSNP Id: rs1578278417

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529050G>T , CM000665.2:g.129529050G>T GRCh38
NC_000003.11:g.129247893G>T , CM000665.1:g.129247893G>T GRCh37
NC_000003.10:g.130730583G>T NCBI36
NG_009115.1:g.5412G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.317G>T MANE Select ENSP00000296271.3:p.Gly106Val
ENST00000296271.3:c.317G>T ENSP00000296271.3:p.Gly106Val
NM_000539.3:c.317G>T MANE Select NP_000530.1:p.Gly106Val