Canonical Allele Identifier: CA354496810
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529039C>A , CM000665.2:g.129529039C>A GRCh38
NC_000003.11:g.129247882C>A , CM000665.1:g.129247882C>A GRCh37
NC_000003.10:g.130730572C>A NCBI36
NG_009115.1:g.5401C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.306C>A MANE Select ENSP00000296271.3:p.Tyr102Ter
ENST00000296271.3:c.306C>A ENSP00000296271.3:p.Tyr102Ter
NM_000539.3:c.306C>A MANE Select NP_000530.1:p.Tyr102Ter