Canonical Allele Identifier: CA1401205856
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528995C= , CM000665.2:g.129528995C= GRCh38
NC_000003.11:g.129247838C= , CM000665.1:g.129247838C= GRCh37
NC_000003.10:g.130730528C= NCBI36
NG_009115.1:g.5357C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.262C= MANE Select ENSP00000296271.3:p.Leu88=
ENST00000296271.3:c.262C= ENSP00000296271.3:p.Leu88=
NM_000539.3:c.262C= MANE Select NP_000530.1:p.Leu88=
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