Canonical Allele Identifier: CA2758363675
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529148_129529149insACA , CM000665.2:g.129529148_129529149insACA GRCh38
NC_000003.11:g.129247991_129247992insACA , CM000665.1:g.129247991_129247992insACA GRCh37
NC_000003.10:g.130730681_130730682insACA NCBI36
NG_009115.1:g.5510_5511insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+54_361+55insACA MANE Select ENSP00000296271.3:n.361+54_361+55insACA
ENST00000296271.3:c.361+54_361+55insACA ENSP00000296271.3:n.361+54_361+55insACA
NM_000539.3:c.361+54_361+55insACA MANE Select NP_000530.1:n.361+54_361+55insACA