Canonical Allele Identifier: CA354498022

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129249755T>A (hg19) ; chr3:g.129530912T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530912T>A , CM000665.2:g.129530912T>A	GRCh38
NC_000003.11:g.129249755T>A , CM000665.1:g.129249755T>A	GRCh37
NC_000003.10:g.130732445T>A	NCBI36
NG_009115.1:g.7274T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.398T>A MANE Select	ENSP00000296271.3:p.Ile133Asn
ENST00000296271.3:c.398T>A	ENSP00000296271.3:p.Ile133Asn
NM_000539.3:c.398T>A MANE Select	NP_000530.1:p.Ile133Asn