Canonical Allele Identifier: CA1401211387
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532436C= , CM000665.2:g.129532436C= GRCh38
NC_000003.11:g.129251279C= , CM000665.1:g.129251279C= GRCh37
NC_000003.10:g.130733969C= NCBI36
NG_009115.1:g.8798C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.696+20C= MANE Select ENSP00000296271.3:n.696+20C=
ENST00000296271.3:c.696+20C= ENSP00000296271.3:n.696+20C=
NM_000539.3:c.696+20C= MANE Select NP_000530.1:n.696+20C=
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