Canonical Allele Identifier: CA1401209234
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530896_129530899delinsTTGG , CM000665.2:g.129530896_129530899delinsTTGG GRCh38
NC_000003.11:g.129249739_129249742delinsTTGG , CM000665.1:g.129249739_129249742delinsTTGG GRCh37
NC_000003.10:g.130732429_130732432delinsTTGG NCBI36
NG_009115.1:g.7258_7261delinsTTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.382_385delinsTTGG MANE Select ENSP00000296271.3:p.Leu128=
ENST00000296271.3:c.382_385delinsTTGG ENSP00000296271.3:p.Leu128=
NM_000539.3:c.382_385delinsTTGG MANE Select NP_000530.1:p.Leu128=