Canonical Allele Identifier: CA2704000729
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2108749901

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530830C>G , CM000665.2:g.129530830C>G GRCh38
NC_000003.11:g.129249673C>G , CM000665.1:g.129249673C>G GRCh37
NC_000003.10:g.130732363C>G NCBI36
NG_009115.1:g.7192C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-46C>G MANE Select ENSP00000296271.3:n.362-46C>G
ENST00000296271.3:c.362-46C>G ENSP00000296271.3:n.362-46C>G
NM_000539.3:c.362-46C>G MANE Select NP_000530.1:n.362-46C>G