Canonical Allele Identifier: CA898752891
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1178949302

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532103del , CM000665.2:g.129532103del GRCh38
NC_000003.11:g.129250946del , CM000665.1:g.129250946del GRCh37
NC_000003.10:g.130733636del NCBI36
NG_009115.1:g.8465del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-148del MANE Select ENSP00000296271.3:n.531-148del
ENST00000296271.3:c.531-148del ENSP00000296271.3:n.531-148del
NM_000539.3:c.531-148del MANE Select NP_000530.1:n.531-148del