Canonical Allele Identifier: CA2704006789

Gene: RHO

Linked Data

• dbSNP Id: rs2108749084

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129528697_129528698insCTA , CM000665.2:g.129528697_129528698insCTA	GRCh38
NC_000003.11:g.129247540_129247541insCTA , CM000665.1:g.129247540_129247541insCTA	GRCh37
NC_000003.10:g.130730230_130730231insCTA	NCBI36
NG_009115.1:g.5059_5060insCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.-37_-36insCTA MANE Select	ENSP00000296271.3:n.-37_-36insCTA
ENST00000296271.3:c.-37_-36insCTA	ENSP00000296271.3:n.-37_-36insCTA
NM_000539.3:c.-37_-36insCTA MANE Select	NP_000530.1:n.-37_-36insCTA