Canonical Allele Identifier: CA82649470
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1027522033
gnomAD v2: 3-129250659-C-A
gnomAD v3: 3-129531816-C-A
gnomAD v4: 3-129531816-C-A
MyVariant Identifiers: chr3:g.129250659C>A (hg19) chr3:g.129531816C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531816C>A , CM000665.2:g.129531816C>A GRCh38
NC_000003.11:g.129250659C>A , CM000665.1:g.129250659C>A GRCh37
NC_000003.10:g.130733349C>A NCBI36
NG_009115.1:g.8178C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-435C>A MANE Select ENSP00000296271.3:n.531-435C>A
ENST00000296271.3:c.531-435C>A ENSP00000296271.3:n.531-435C>A
NM_000539.3:c.531-435C>A MANE Select NP_000530.1:n.531-435C>A
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