Canonical Allele Identifier: CA2758363736
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529204_129529205insACTT , CM000665.2:g.129529204_129529205insACTT GRCh38
NC_000003.11:g.129248047_129248048insACTT , CM000665.1:g.129248047_129248048insACTT GRCh37
NC_000003.10:g.130730737_130730738insACTT NCBI36
NG_009115.1:g.5566_5567insACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+110_361+111insACTT MANE Select ENSP00000296271.3:n.361+110_361+111insACTT
ENST00000296271.3:c.361+110_361+111insACTT ENSP00000296271.3:n.361+110_361+111insACTT
NM_000539.3:c.361+110_361+111insACTT MANE Select NP_000530.1:n.361+110_361+111insACTT
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