Canonical Allele Identifier: CA354470039
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129251232T>G (hg19) chr3:g.129532389T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532389T>G , CM000665.2:g.129532389T>G GRCh38
NC_000003.11:g.129251232T>G , CM000665.1:g.129251232T>G GRCh37
NC_000003.10:g.130733922T>G NCBI36
NG_009115.1:g.8751T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.669T>G MANE Select ENSP00000296271.3:p.Tyr223Ter
ENST00000296271.3:c.669T>G ENSP00000296271.3:p.Tyr223Ter
NM_000539.3:c.669T>G MANE Select NP_000530.1:p.Tyr223Ter
Search 100 bp 5'
Search 100 bp 3'