Canonical Allele Identifier: CA1401206313

Gene: RHO

Linked Data

• dbSNP Id: rs376995477

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129529105_129529106del , CM000665.2:g.129529105_129529106del	GRCh38
NC_000003.11:g.129247948_129247949del , CM000665.1:g.129247948_129247949del	GRCh37
NC_000003.10:g.130730638_130730639del	NCBI36
NG_009115.1:g.5467_5468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.361+11_361+12del MANE Select	ENSP00000296271.3:n.361+11_361+12del
ENST00000296271.3:c.361+11_361+12del	ENSP00000296271.3:n.361+11_361+12del
NM_000539.3:c.361+11_361+12del MANE Select	NP_000530.1:n.361+11_361+12del