Canonical Allele Identifier: CA1401205904
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529000T= , CM000665.2:g.129529000T= GRCh38
NC_000003.11:g.129247843T= , CM000665.1:g.129247843T= GRCh37
NC_000003.10:g.130730533T= NCBI36
NG_009115.1:g.5362T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.267T= MANE Select ENSP00000296271.3:p.Gly89=
ENST00000296271.3:c.267T= ENSP00000296271.3:p.Gly89=
NM_000539.3:c.267T= MANE Select NP_000530.1:p.Gly89=