Canonical Allele Identifier: CA898751568
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1257173881
gnomAD v3: 3-129530567-C-CACAA
gnomAD v4: 3-129530567-C-CACAA
MyVariant Identifiers: chr3:g.129249410_129249411insACAA (hg19) chr3:g.129530567_129530568insACAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530568_129530569insCAAA , CM000665.2:g.129530568_129530569insCAAA GRCh38
NC_000003.11:g.129249411_129249412insCAAA , CM000665.1:g.129249411_129249412insCAAA GRCh37
NC_000003.10:g.130732101_130732102insCAAA NCBI36
NG_009115.1:g.6930_6931insCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-308_362-307insCAAA MANE Select ENSP00000296271.3:n.362-308_362-307insCAAA
ENST00000296271.3:c.362-308_362-307insCAAA ENSP00000296271.3:n.362-308_362-307insCAAA
NM_000539.3:c.362-308_362-307insCAAA MANE Select NP_000530.1:n.362-308_362-307insCAAA
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Search 100 bp 3'