Canonical Allele Identifier: CA2758363787
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529225_129529228del , CM000665.2:g.129529225_129529228del GRCh38
NC_000003.11:g.129248068_129248071del , CM000665.1:g.129248068_129248071del GRCh37
NC_000003.10:g.130730758_130730761del NCBI36
NG_009115.1:g.5587_5590del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+131_361+134del MANE Select ENSP00000296271.3:n.361+131_361+134del
ENST00000296271.3:c.361+131_361+134del ENSP00000296271.3:n.361+131_361+134del
NM_000539.3:c.361+131_361+134del MANE Select NP_000530.1:n.361+131_361+134del