Canonical Allele Identifier: CA1401209238
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084774819

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530901_129530903del , CM000665.2:g.129530901_129530903del GRCh38
NC_000003.11:g.129249744_129249746del , CM000665.1:g.129249744_129249746del GRCh37
NC_000003.10:g.130732434_130732436del NCBI36
NG_009115.1:g.7263_7265del

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.387_389del MANE Select ENSP00000296271.3:p.Val130del
ENST00000296271.3:c.387_389del ENSP00000296271.3:p.Val130del
NM_000539.3:c.387_389del MANE Select NP_000530.1:p.Val130del