Canonical Allele Identifier: CA1401210588
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084783522
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531983A>C , CM000665.2:g.129531983A>C GRCh38
NC_000003.11:g.129250826A>C , CM000665.1:g.129250826A>C GRCh37
NC_000003.10:g.130733516A>C NCBI36
NG_009115.1:g.8345A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-268A>C MANE Select ENSP00000296271.3:n.531-268A>C
ENST00000296271.3:c.531-268A>C ENSP00000296271.3:n.531-268A>C
NM_000539.3:c.531-268A>C MANE Select NP_000530.1:n.531-268A>C
Search 100 bp 5'
Search 100 bp 3'