Canonical Allele Identifier: CA1053435581
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs60120581
gnomAD v3: 3-129530533-A-AACACACACACACACACACACACACAC
gnomAD v4: 3-129530533-A-AACACACACACACACACACACACACAC
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530543_129530568dup , CM000665.2:g.129530543_129530568dup GRCh38
NC_000003.11:g.129249386_129249411dup , CM000665.1:g.129249386_129249411dup GRCh37
NC_000003.10:g.130732076_130732101dup NCBI36
NG_009115.1:g.6905_6930dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-333_362-308dup MANE Select ENSP00000296271.3:n.362-333_362-308dup
ENST00000296271.3:c.362-333_362-308dup ENSP00000296271.3:n.362-333_362-308dup
NM_000539.3:c.362-333_362-308dup MANE Select NP_000530.1:n.362-333_362-308dup
Search 100 bp 5'
Search 100 bp 3'