Canonical Allele Identifier: CA1401211213
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532347G= , CM000665.2:g.129532347G= GRCh38
NC_000003.11:g.129251190G= , CM000665.1:g.129251190G= GRCh37
NC_000003.10:g.130733880G= NCBI36
NG_009115.1:g.8709G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.627G= MANE Select ENSP00000296271.3:p.Val209=
ENST00000296271.3:c.627G= ENSP00000296271.3:p.Val209=
NM_000539.3:c.627G= MANE Select NP_000530.1:p.Val209=