Canonical Allele Identifier: CA435768863
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1578278108
MyVariant Identifiers: chr3:g.129247630T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528787T>C , CM000665.2:g.129528787T>C GRCh38
NC_000003.11:g.129247630T>C , CM000665.1:g.129247630T>C GRCh37
NC_000003.10:g.130730320T>C NCBI36
NG_009115.1:g.5149T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.54T>C MANE Select ENSP00000296271.3:p.Gly18=
ENST00000296271.3:c.54T>C ENSP00000296271.3:p.Gly18=
NM_000539.3:c.54T>C MANE Select NP_000530.1:p.Gly18=
Search 100 bp 5'
Search 100 bp 3'