Canonical Allele Identifier: CA1401209199
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530880A= , CM000665.2:g.129530880A= GRCh38
NC_000003.11:g.129249723A= , CM000665.1:g.129249723A= GRCh37
NC_000003.10:g.130732413A= NCBI36
NG_009115.1:g.7242A=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.366A= MANE Select ENSP00000296271.3:p.Glu122=
ENST00000296271.3:c.366A= ENSP00000296271.3:p.Glu122=
NM_000539.3:c.366A= MANE Select NP_000530.1:p.Glu122=