Canonical Allele Identifier: CA2758363684

Gene: RHO

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129529173_129529174insACA , CM000665.2:g.129529173_129529174insACA	GRCh38
NC_000003.11:g.129248016_129248017insACA , CM000665.1:g.129248016_129248017insACA	GRCh37
NC_000003.10:g.130730706_130730707insACA	NCBI36
NG_009115.1:g.5535_5536insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.361+79_361+80insACA MANE Select	ENSP00000296271.3:n.361+79_361+80insACA
ENST00000296271.3:c.361+79_361+80insACA	ENSP00000296271.3:n.361+79_361+80insACA
NM_000539.3:c.361+79_361+80insACA MANE Select	NP_000530.1:n.361+79_361+80insACA