Canonical Allele Identifier: CA1401212190
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084793513
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532777C>G , CM000665.2:g.129532777C>G GRCh38
NC_000003.11:g.129251620C>G , CM000665.1:g.129251620C>G GRCh37
NC_000003.10:g.130734310C>G NCBI36
NG_009115.1:g.9139C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.936+5C>G MANE Select ENSP00000296271.3:n.936+5C>G
ENST00000296271.3:c.936+5C>G ENSP00000296271.3:n.936+5C>G
NM_000539.3:c.936+5C>G MANE Select NP_000530.1:n.936+5C>G
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