Canonical Allele Identifier: CA354498298
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530965A>T , CM000665.2:g.129530965A>T GRCh38
NC_000003.11:g.129249808A>T , CM000665.1:g.129249808A>T GRCh37
NC_000003.10:g.130732498A>T NCBI36
NG_009115.1:g.7327A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.451A>T MANE Select ENSP00000296271.3:p.Asn151Tyr
ENST00000296271.3:c.451A>T ENSP00000296271.3:p.Asn151Tyr
NM_000539.3:c.451A>T MANE Select NP_000530.1:p.Asn151Tyr