Canonical Allele Identifier: CA1401208813
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084771717

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530535_129530537del , CM000665.2:g.129530535_129530537del GRCh38
NC_000003.11:g.129249378_129249380del , CM000665.1:g.129249378_129249380del GRCh37
NC_000003.10:g.130732068_130732070del NCBI36
NG_009115.1:g.6897_6899del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-341_362-339del MANE Select ENSP00000296271.3:n.362-341_362-339del
ENST00000296271.3:c.362-341_362-339del ENSP00000296271.3:n.362-341_362-339del
NM_000539.3:c.362-341_362-339del MANE Select NP_000530.1:n.362-341_362-339del