Canonical Allele Identifier: CA2758363836
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529293_129529294insAC , CM000665.2:g.129529293_129529294insAC GRCh38
NC_000003.11:g.129248136_129248137insAC , CM000665.1:g.129248136_129248137insAC GRCh37
NC_000003.10:g.130730826_130730827insAC NCBI36
NG_009115.1:g.5655_5656insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+199_361+200insAC MANE Select ENSP00000296271.3:n.361+199_361+200insAC
ENST00000296271.3:c.361+199_361+200insAC ENSP00000296271.3:n.361+199_361+200insAC
NM_000539.3:c.361+199_361+200insAC MANE Select NP_000530.1:n.361+199_361+200insAC