Canonical Allele Identifier: CA354495868
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1287941897

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528863A>G , CM000665.2:g.129528863A>G GRCh38
NC_000003.11:g.129247706A>G , CM000665.1:g.129247706A>G GRCh37
NC_000003.10:g.130730396A>G NCBI36
NG_009115.1:g.5225A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.130A>G MANE Select ENSP00000296271.3:p.Met44Val
ENST00000296271.3:c.130A>G ENSP00000296271.3:p.Met44Val
NM_000539.3:c.130A>G MANE Select NP_000530.1:p.Met44Val