Canonical Allele Identifier: CA546228066
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1257173881
gnomAD v2: 3-129249410-C-CACACACACACACAA
gnomAD v3: 3-129530567-C-CACACACACACACAA
gnomAD v4: 3-129530567-C-CACACACACACACAA
MyVariant Identifiers: chr3:g.129249410_129249411insACACACACACACAA (hg19) chr3:g.129530567_129530568insACACACACACACAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530568_129530569insCACACACACACAAA , CM000665.2:g.129530568_129530569insCACACACACACAAA GRCh38
NC_000003.11:g.129249411_129249412insCACACACACACAAA , CM000665.1:g.129249411_129249412insCACACACACACAAA GRCh37
NC_000003.10:g.130732101_130732102insCACACACACACAAA NCBI36
NG_009115.1:g.6930_6931insCACACACACACAAA

Transcript Alleles

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