Canonical Allele Identifier: CA898750798

Gene: RHO

Linked Data

• dbSNP Id: rs1407721146
• MyVariant Identifiers: chr3:g.129248231_129248232insG (hg19) ; chr3:g.129529388_129529389insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129529392dup , CM000665.2:g.129529392dup	GRCh38
NC_000003.11:g.129248235dup , CM000665.1:g.129248235dup	GRCh37
NC_000003.10:g.130730925dup	NCBI36
NG_009115.1:g.5754dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.361+298dup MANE Select	ENSP00000296271.3:n.361+298dup
ENST00000296271.3:c.361+298dup	ENSP00000296271.3:n.361+298dup
NM_000539.3:c.361+298dup MANE Select	NP_000530.1:n.361+298dup