Canonical Allele Identifier: CA2607144
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs764607760

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530873C>T , CM000665.2:g.129530873C>T GRCh38
NC_000003.11:g.129249716C>T , CM000665.1:g.129249716C>T GRCh37
NC_000003.10:g.130732406C>T NCBI36
NG_009115.1:g.7235C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-3C>T MANE Select ENSP00000296271.3:n.362-3C>T
ENST00000296271.3:c.362-3C>T ENSP00000296271.3:n.362-3C>T
NM_000539.3:c.362-3C>T MANE Select NP_000530.1:n.362-3C>T