Canonical Allele Identifier: CA354496864
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 956525
ClinVar RCV Id: RCV001229349
dbSNP Id: rs104893773
MyVariant Identifiers: chr3:g.129247892G>C (hg19) chr3:g.129529049G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529049G>C , CM000665.2:g.129529049G>C GRCh38
NC_000003.11:g.129247892G>C , CM000665.1:g.129247892G>C GRCh37
NC_000003.10:g.130730582G>C NCBI36
NG_009115.1:g.5411G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.316G>C MANE Select ENSP00000296271.3:p.Gly106Arg
ENST00000296271.3:c.316G>C ENSP00000296271.3:p.Gly106Arg
NM_000539.3:c.316G>C MANE Select NP_000530.1:p.Gly106Arg
Search 100 bp 5'
Search 100 bp 3'