Canonical Allele Identifier: CA1401205830
Gene: RHO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528985C= , CM000665.2:g.129528985C= GRCh38
NC_000003.11:g.129247828C= , CM000665.1:g.129247828C= GRCh37
NC_000003.10:g.130730518C= NCBI36
NG_009115.1:g.5347C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.252C= MANE Select ENSP00000296271.3:p.Leu84=
ENST00000296271.3:c.252C= ENSP00000296271.3:p.Leu84=
NM_000539.3:c.252C= MANE Select NP_000530.1:p.Leu84=
Search 100 bp 5'
Search 100 bp 3'