Canonical Allele Identifier: CA435768986
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1488045716

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532347G>T , CM000665.2:g.129532347G>T GRCh38
NC_000003.11:g.129251190G>T , CM000665.1:g.129251190G>T GRCh37
NC_000003.10:g.130733880G>T NCBI36
NG_009115.1:g.8709G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.627G>T MANE Select ENSP00000296271.3:p.Val209=
ENST00000296271.3:c.627G>T ENSP00000296271.3:p.Val209=
NM_000539.3:c.627G>T MANE Select NP_000530.1:p.Val209=