Canonical Allele Identifier: CA354496329
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528950A>T , CM000665.2:g.129528950A>T GRCh38
NC_000003.11:g.129247793A>T , CM000665.1:g.129247793A>T GRCh37
NC_000003.10:g.130730483A>T NCBI36
NG_009115.1:g.5312A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.217A>T MANE Select ENSP00000296271.3:p.Asn73Tyr
ENST00000296271.3:c.217A>T ENSP00000296271.3:p.Asn73Tyr
NM_000539.3:c.217A>T MANE Select NP_000530.1:p.Asn73Tyr