Canonical Allele Identifier: CA354499040
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532249A>C , CM000665.2:g.129532249A>C GRCh38
NC_000003.11:g.129251092A>C , CM000665.1:g.129251092A>C GRCh37
NC_000003.10:g.130733782A>C NCBI36
NG_009115.1:g.8611A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.531-2A>C MANE Select ENSP00000296271.3:n.531-2A>C
ENST00000296271.3:c.531-2A>C ENSP00000296271.3:n.531-2A>C
NM_000539.3:c.531-2A>C MANE Select NP_000530.1:n.531-2A>C