Canonical Allele Identifier: CA2758363707
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529191_129529192insACA , CM000665.2:g.129529191_129529192insACA GRCh38
NC_000003.11:g.129248034_129248035insACA , CM000665.1:g.129248034_129248035insACA GRCh37
NC_000003.10:g.130730724_130730725insACA NCBI36
NG_009115.1:g.5553_5554insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+97_361+98insACA MANE Select ENSP00000296271.3:n.361+97_361+98insACA
ENST00000296271.3:c.361+97_361+98insACA ENSP00000296271.3:n.361+97_361+98insACA
NM_000539.3:c.361+97_361+98insACA MANE Select NP_000530.1:n.361+97_361+98insACA