Canonical Allele Identifier: CA1401208156
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084770598
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530516del , CM000665.2:g.129530516del GRCh38
NC_000003.11:g.129249359del , CM000665.1:g.129249359del GRCh37
NC_000003.10:g.130732049del NCBI36
NG_009115.1:g.6878del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-360del MANE Select ENSP00000296271.3:n.362-360del
ENST00000296271.3:c.362-360del ENSP00000296271.3:n.362-360del
NM_000539.3:c.362-360del MANE Select NP_000530.1:n.362-360del
Search 100 bp 5'
Search 100 bp 3'