Canonical Allele Identifier: CA1401213248
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129533652A= , CM000665.2:g.129533652A= GRCh38
NC_000003.11:g.129252495A= , CM000665.1:g.129252495A= GRCh37
NC_000003.10:g.130735185A= NCBI36
NG_009115.1:g.10014A=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.981A= MANE Select ENSP00000296271.3:p.Pro327=
ENST00000296271.3:c.981A= ENSP00000296271.3:p.Pro327=
NM_000539.3:c.981A= MANE Select NP_000530.1:p.Pro327=