Canonical Allele Identifier: CA1401210919
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532265_129532266delinsGC , CM000665.2:g.129532265_129532266delinsGC GRCh38
NC_000003.11:g.129251108_129251109delinsGC , CM000665.1:g.129251108_129251109delinsGC GRCh37
NC_000003.10:g.130733798_130733799delinsGC NCBI36
NG_009115.1:g.8627_8628delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.545_546delinsGC MANE Select ENSP00000296271.3:p.Gly182=
ENST00000296271.3:c.545_546delinsGC ENSP00000296271.3:p.Gly182=
NM_000539.3:c.545_546delinsGC MANE Select NP_000530.1:p.Gly182=