Canonical Allele Identifier: CA1053435783
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084772209
gnomAD v3: 3-129530567-C-CAA
gnomAD v4: 3-129530567-C-CAA
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530570_129530571dup , CM000665.2:g.129530570_129530571dup GRCh38
NC_000003.11:g.129249413_129249414dup , CM000665.1:g.129249413_129249414dup GRCh37
NC_000003.10:g.130732103_130732104dup NCBI36
NG_009115.1:g.6932_6933dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-306_362-305dup MANE Select ENSP00000296271.3:n.362-306_362-305dup
ENST00000296271.3:c.362-306_362-305dup ENSP00000296271.3:n.362-306_362-305dup
NM_000539.3:c.362-306_362-305dup MANE Select NP_000530.1:n.362-306_362-305dup
Search 100 bp 5'
Search 100 bp 3'