Canonical Allele Identifier: CA2607091
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs758491851

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528953T>C , CM000665.2:g.129528953T>C GRCh38
NC_000003.11:g.129247796T>C , CM000665.1:g.129247796T>C GRCh37
NC_000003.10:g.130730486T>C NCBI36
NG_009115.1:g.5315T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.220T>C MANE Select ENSP00000296271.3:p.Tyr74His
ENST00000296271.3:c.220T>C ENSP00000296271.3:p.Tyr74His
NM_000539.3:c.220T>C MANE Select NP_000530.1:p.Tyr74His