Canonical Allele Identifier: CA1053435131
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084771058
gnomAD v3: 3-129530529-A-AC
gnomAD v4: 3-129530529-A-AC
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530530dup , CM000665.2:g.129530530dup GRCh38
NC_000003.11:g.129249373dup , CM000665.1:g.129249373dup GRCh37
NC_000003.10:g.130732063dup NCBI36
NG_009115.1:g.6892dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-346dup MANE Select ENSP00000296271.3:n.362-346dup
ENST00000296271.3:c.362-346dup ENSP00000296271.3:n.362-346dup
NM_000539.3:c.362-346dup MANE Select NP_000530.1:n.362-346dup
Search 100 bp 5'
Search 100 bp 3'