Canonical Allele Identifier: CA354498282

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129249805G>T (hg19) ; chr3:g.129530962G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530962G>T , CM000665.2:g.129530962G>T	GRCh38
NC_000003.11:g.129249805G>T , CM000665.1:g.129249805G>T	GRCh37
NC_000003.10:g.130732495G>T	NCBI36
NG_009115.1:g.7324G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.448G>T MANE Select	ENSP00000296271.3:p.Glu150Ter
ENST00000296271.3:c.448G>T	ENSP00000296271.3:p.Glu150Ter
NM_000539.3:c.448G>T MANE Select	NP_000530.1:p.Glu150Ter