Canonical Allele Identifier: CA2581897357
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528708A>C , CM000665.2:g.129528708A>C GRCh38
NC_000003.11:g.129247551A>C , CM000665.1:g.129247551A>C GRCh37
NC_000003.10:g.130730241A>C NCBI36
NG_009115.1:g.5070A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-26A>C MANE Select ENSP00000296271.3:n.-26A>C
ENST00000296271.3:c.-26A>C ENSP00000296271.3:n.-26A>C
NM_000539.3:c.-26A>C MANE Select NP_000530.1:n.-26A>C
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