Canonical Allele Identifier: CA354496878
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529053C>G , CM000665.2:g.129529053C>G GRCh38
NC_000003.11:g.129247896C>G , CM000665.1:g.129247896C>G GRCh37
NC_000003.10:g.130730586C>G NCBI36
NG_009115.1:g.5415C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.320C>G MANE Select ENSP00000296271.3:p.Pro107Arg
ENST00000296271.3:c.320C>G ENSP00000296271.3:p.Pro107Arg
NM_000539.3:c.320C>G MANE Select NP_000530.1:p.Pro107Arg