Canonical Allele Identifier: CA2758363691
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529177_129529178insACAT , CM000665.2:g.129529177_129529178insACAT GRCh38
NC_000003.11:g.129248020_129248021insACAT , CM000665.1:g.129248020_129248021insACAT GRCh37
NC_000003.10:g.130730710_130730711insACAT NCBI36
NG_009115.1:g.5539_5540insACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+83_361+84insACAT MANE Select ENSP00000296271.3:n.361+83_361+84insACAT
ENST00000296271.3:c.361+83_361+84insACAT ENSP00000296271.3:n.361+83_361+84insACAT
NM_000539.3:c.361+83_361+84insACAT MANE Select NP_000530.1:n.361+83_361+84insACAT