Canonical Allele Identifier: CA1401210607
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084783701
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532022_129532030del , CM000665.2:g.129532022_129532030del GRCh38
NC_000003.11:g.129250865_129250873del , CM000665.1:g.129250865_129250873del GRCh37
NC_000003.10:g.130733555_130733563del NCBI36
NG_009115.1:g.8384_8392del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-229_531-221del MANE Select ENSP00000296271.3:n.531-229_531-221del
ENST00000296271.3:c.531-229_531-221del ENSP00000296271.3:n.531-229_531-221del
NM_000539.3:c.531-229_531-221del MANE Select NP_000530.1:n.531-229_531-221del
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Search 100 bp 3'