Canonical Allele Identifier: CA2604332638
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2108750216
gnomAD v3: 3-129531846-TC-T
gnomAD v4: 3-129531846-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531847del , CM000665.2:g.129531847del GRCh38
NC_000003.11:g.129250690del , CM000665.1:g.129250690del GRCh37
NC_000003.10:g.130733380del NCBI36
NG_009115.1:g.8209del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-404del MANE Select ENSP00000296271.3:n.531-404del
ENST00000296271.3:c.531-404del ENSP00000296271.3:n.531-404del
NM_000539.3:c.531-404del MANE Select NP_000530.1:n.531-404del
Search 100 bp 5'
Search 100 bp 3'