Canonical Allele Identifier: CA546228077
Gene: RHO HGNC NCBI

Linked Data

gnomAD v2: 3-129249411-A-ACACACACACACACACACACACACACAC
gnomAD v3: 3-129530568-A-ACACACACACACACACACACACACACAC
gnomAD v4: 3-129530568-A-ACACACACACACACACACACACACACAC
MyVariant Identifiers: chr3:g.129249411_129249412insCACACACACACACACACACACACACAC (hg19) chr3:g.129530568_129530569insCACACACACACACACACACACACACAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530568_129530569insCACACACACACACACACACACACACAC , CM000665.2:g.129530568_129530569insCACACACACACACACACACACACACAC GRCh38
NC_000003.11:g.129249411_129249412insCACACACACACACACACACACACACAC , CM000665.1:g.129249411_129249412insCACACACACACACACACACACACACAC GRCh37
NC_000003.10:g.130732101_130732102insCACACACACACACACACACACACACAC NCBI36
NG_009115.1:g.6930_6931insCACACACACACACACACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-308_362-307insCACACACACACACACACACACACACAC MANE Select ENSP00000296271.3:n.362-308_362-307insCACACACACACACACACACACAC...
ENST00000296271.3:c.362-308_362-307insCACACACACACACACACACACACACAC ENSP00000296271.3:n.362-308_362-307insCACACACACACACACACACACAC...
NM_000539.3:c.362-308_362-307insCACACACACACACACACACACACACAC MANE Select NP_000530.1:n.362-308_362-307insCACACACACACACACACACACACACAC
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