Canonical Allele Identifier: CA2704002181
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2108750205
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531795del , CM000665.2:g.129531795del GRCh38
NC_000003.11:g.129250638del , CM000665.1:g.129250638del GRCh37
NC_000003.10:g.130733328del NCBI36
NG_009115.1:g.8157del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-456del MANE Select ENSP00000296271.3:n.531-456del
ENST00000296271.3:c.531-456del ENSP00000296271.3:n.531-456del
NM_000539.3:c.531-456del MANE Select NP_000530.1:n.531-456del
Search 100 bp 5'
Search 100 bp 3'