Canonical Allele Identifier: CA546228072
Gene: RHO HGNC NCBI

Linked Data

gnomAD v2: 3-129249411-A-ACACACACACACACACACACAC
gnomAD v3: 3-129530568-A-ACACACACACACACACACACAC
gnomAD v4: 3-129530568-A-ACACACACACACACACACACAC
MyVariant Identifiers: chr3:g.129249411_129249412insCACACACACACACACACACAC (hg19) chr3:g.129530568_129530569insCACACACACACACACACACAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530568_129530569insCACACACACACACACACACAC , CM000665.2:g.129530568_129530569insCACACACACACACACACACAC GRCh38
NC_000003.11:g.129249411_129249412insCACACACACACACACACACAC , CM000665.1:g.129249411_129249412insCACACACACACACACACACAC GRCh37
NC_000003.10:g.130732101_130732102insCACACACACACACACACACAC NCBI36
NG_009115.1:g.6930_6931insCACACACACACACACACACAC

Transcript Alleles

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