Canonical Allele Identifier: CA2758363710
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529193_129529194insAG , CM000665.2:g.129529193_129529194insAG GRCh38
NC_000003.11:g.129248036_129248037insAG , CM000665.1:g.129248036_129248037insAG GRCh37
NC_000003.10:g.130730726_130730727insAG NCBI36
NG_009115.1:g.5555_5556insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+99_361+100insAG MANE Select ENSP00000296271.3:n.361+99_361+100insAG
ENST00000296271.3:c.361+99_361+100insAG ENSP00000296271.3:n.361+99_361+100insAG
NM_000539.3:c.361+99_361+100insAG MANE Select NP_000530.1:n.361+99_361+100insAG