Canonical Allele Identifier: CA354470349

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129251460T>G (hg19) ; chr3:g.129532617T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129532617T>G , CM000665.2:g.129532617T>G	GRCh38
NC_000003.11:g.129251460T>G , CM000665.1:g.129251460T>G	GRCh37
NC_000003.10:g.130734150T>G	NCBI36
NG_009115.1:g.8979T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.781T>G MANE Select	ENSP00000296271.3:p.Phe261Val
ENST00000296271.3:c.781T>G	ENSP00000296271.3:p.Phe261Val
NM_000539.3:c.781T>G MANE Select	NP_000530.1:p.Phe261Val