Canonical Allele Identifier: CA898751652

Gene: RHO

Linked Data

• dbSNP Id: rs1473773483
• MyVariant Identifiers: chr3:g.129249524C>G (hg19) ; chr3:g.129530681C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530681C>G , CM000665.2:g.129530681C>G	GRCh38
NC_000003.11:g.129249524C>G , CM000665.1:g.129249524C>G	GRCh37
NC_000003.10:g.130732214C>G	NCBI36
NG_009115.1:g.7043C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.362-195C>G MANE Select	ENSP00000296271.3:n.362-195C>G
ENST00000296271.3:c.362-195C>G	ENSP00000296271.3:n.362-195C>G
NM_000539.3:c.362-195C>G MANE Select	NP_000530.1:n.362-195C>G