Canonical Allele Identifier: CA1053435831
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084772349
gnomAD v3: 3-129530573-T-A
gnomAD v4: 3-129530573-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530573T>A , CM000665.2:g.129530573T>A GRCh38
NC_000003.11:g.129249416T>A , CM000665.1:g.129249416T>A GRCh37
NC_000003.10:g.130732106T>A NCBI36
NG_009115.1:g.6935T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-303T>A MANE Select ENSP00000296271.3:n.362-303T>A
ENST00000296271.3:c.362-303T>A ENSP00000296271.3:n.362-303T>A
NM_000539.3:c.362-303T>A MANE Select NP_000530.1:n.362-303T>A
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