Canonical Allele Identifier: CA1401208066
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084769940
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530449del , CM000665.2:g.129530449del GRCh38
NC_000003.11:g.129249292del , CM000665.1:g.129249292del GRCh37
NC_000003.10:g.130731982del NCBI36
NG_009115.1:g.6811del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-427del MANE Select ENSP00000296271.3:n.362-427del
ENST00000296271.3:c.362-427del ENSP00000296271.3:n.362-427del
NM_000539.3:c.362-427del MANE Select NP_000530.1:n.362-427del
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Search 100 bp 3'