Canonical Allele Identifier: CA1401205509
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528906C= , CM000665.2:g.129528906C= GRCh38
NC_000003.11:g.129247749C= , CM000665.1:g.129247749C= GRCh37
NC_000003.10:g.130730439C= NCBI36
NG_009115.1:g.5268C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.173C= MANE Select ENSP00000296271.3:p.Thr58=
ENST00000296271.3:c.173C= ENSP00000296271.3:p.Thr58=
NM_000539.3:c.173C= MANE Select NP_000530.1:p.Thr58=