Canonical Allele Identifier: CA435768725
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129247840A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528997A>T , CM000665.2:g.129528997A>T GRCh38
NC_000003.11:g.129247840A>T , CM000665.1:g.129247840A>T GRCh37
NC_000003.10:g.130730530A>T NCBI36
NG_009115.1:g.5359A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.264A>T MANE Select ENSP00000296271.3:p.Leu88=
ENST00000296271.3:c.264A>T ENSP00000296271.3:p.Leu88=
NM_000539.3:c.264A>T MANE Select NP_000530.1:p.Leu88=
Search 100 bp 5'
Search 100 bp 3'