Canonical Allele Identifier: CA354470342

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129251455T>G (hg19) ; chr3:g.129532612T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129532612T>G , CM000665.2:g.129532612T>G	GRCh38
NC_000003.11:g.129251455T>G , CM000665.1:g.129251455T>G	GRCh37
NC_000003.10:g.130734145T>G	NCBI36
NG_009115.1:g.8974T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.776T>G MANE Select	ENSP00000296271.3:p.Ile259Ser
ENST00000296271.3:c.776T>G	ENSP00000296271.3:p.Ile259Ser
NM_000539.3:c.776T>G MANE Select	NP_000530.1:p.Ile259Ser