Canonical Allele Identifier: CA1401208831
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530540_129530541delinsAC , CM000665.2:g.129530540_129530541delinsAC GRCh38
NC_000003.11:g.129249383_129249384delinsAC , CM000665.1:g.129249383_129249384delinsAC GRCh37
NC_000003.10:g.130732073_130732074delinsAC NCBI36
NG_009115.1:g.6902_6903delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-336_362-335delinsAC MANE Select ENSP00000296271.3:n.362-336_362-335delinsAC
ENST00000296271.3:c.362-336_362-335delinsAC ENSP00000296271.3:n.362-336_362-335delinsAC
NM_000539.3:c.362-336_362-335delinsAC MANE Select NP_000530.1:n.362-336_362-335delinsAC