Canonical Allele Identifier: CA648379652
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528708_129528709insG , CM000665.2:g.129528708_129528709insG GRCh38
NC_000003.11:g.129247551_129247552insG , CM000665.1:g.129247551_129247552insG GRCh37
NC_000003.10:g.130730241_130730242insG NCBI36
NG_009115.1:g.5070_5071insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-26_-25insG MANE Select ENSP00000296271.3:n.-26_-25insG
ENST00000296271.3:c.-26_-25insG ENSP00000296271.3:n.-26_-25insG
NM_000539.3:c.-26_-25insG MANE Select NP_000530.1:n.-26_-25insG