Canonical Allele Identifier: CA1401211218
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532348G= , CM000665.2:g.129532348G= GRCh38
NC_000003.11:g.129251191G= , CM000665.1:g.129251191G= GRCh37
NC_000003.10:g.130733881G= NCBI36
NG_009115.1:g.8710G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.628G= MANE Select ENSP00000296271.3:p.Val210=
ENST00000296271.3:c.628G= ENSP00000296271.3:p.Val210=
NM_000539.3:c.628G= MANE Select NP_000530.1:p.Val210=