Canonical Allele Identifier: CA354498321
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530968C>G , CM000665.2:g.129530968C>G GRCh38
NC_000003.11:g.129249811C>G , CM000665.1:g.129249811C>G GRCh37
NC_000003.10:g.130732501C>G NCBI36
NG_009115.1:g.7330C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.454C>G MANE Select ENSP00000296271.3:p.His152Asp
ENST00000296271.3:c.454C>G ENSP00000296271.3:p.His152Asp
NM_000539.3:c.454C>G MANE Select NP_000530.1:p.His152Asp