Canonical Allele Identifier: CA546228068
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1257173881
gnomAD v2: 3-129249410-C-CACACACACACACACACACAA
gnomAD v3: 3-129530567-C-CACACACACACACACACACAA
gnomAD v4: 3-129530567-C-CACACACACACACACACACAA
MyVariant Identifiers: chr3:g.129249410_129249411insACACACACACACACACACAA (hg19) chr3:g.129530567_129530568insACACACACACACACACACAA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530568_129530569insCACACACACACACACACAAA , CM000665.2:g.129530568_129530569insCACACACACACACACACAAA GRCh38
NC_000003.11:g.129249411_129249412insCACACACACACACACACAAA , CM000665.1:g.129249411_129249412insCACACACACACACACACAAA GRCh37
NC_000003.10:g.130732101_130732102insCACACACACACACACACAAA NCBI36
NG_009115.1:g.6930_6931insCACACACACACACACACAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-308_362-307insCACACACACACACACACAAA MANE Select ENSP00000296271.3:n.362-308_362-307insCACACACACACACACACAAA
ENST00000296271.3:c.362-308_362-307insCACACACACACACACACAAA ENSP00000296271.3:n.362-308_362-307insCACACACACACACACACAAA
NM_000539.3:c.362-308_362-307insCACACACACACACACACAAA MANE Select NP_000530.1:n.362-308_362-307insCACACACACACACACACAAA
Search 100 bp 5'
Search 100 bp 3'