Canonical Allele Identifier: CA1401208050
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530418G= , CM000665.2:g.129530418G= GRCh38
NC_000003.11:g.129249261G= , CM000665.1:g.129249261G= GRCh37
NC_000003.10:g.130731951G= NCBI36
NG_009115.1:g.6780G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-458G= MANE Select ENSP00000296271.3:n.362-458G=
ENST00000296271.3:c.362-458G= ENSP00000296271.3:n.362-458G=
NM_000539.3:c.362-458G= MANE Select NP_000530.1:n.362-458G=
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