Canonical Allele Identifier: CA435768949
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129247750G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528907G>C , CM000665.2:g.129528907G>C GRCh38
NC_000003.11:g.129247750G>C , CM000665.1:g.129247750G>C GRCh37
NC_000003.10:g.130730440G>C NCBI36
NG_009115.1:g.5269G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.174G>C MANE Select ENSP00000296271.3:p.Thr58=
ENST00000296271.3:c.174G>C ENSP00000296271.3:p.Thr58=
NM_000539.3:c.174G>C MANE Select NP_000530.1:p.Thr58=
Search 100 bp 5'
Search 100 bp 3'