Canonical Allele Identifier: CA1877946346

Gene: CRB2

Linked Data

• dbSNP Id: rs2042110208

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376855_123376860dup , CM000671.2:g.123376855_123376860dup	GRCh38
NC_000009.11:g.126139134_126139139dup , CM000671.1:g.126139134_126139139dup	GRCh37
NC_000009.10:g.125178955_125178960dup	NCBI36
NG_051311.1:g.27791_27796dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3651_3656dup MANE Select	ENSP00000362734.3:p.Pro1219_Phe1220insLeuPro
ENST00000373631.7:c.3651_3656dup	ENSP00000362734.3:p.Pro1219_Phe1220insLeuPro
ENST00000460253.1:c.2655_2660dup	ENSP00000435279.1:p.Pro887_Phe888insLeuPro
NM_173689.6:c.3651_3656dup	NP_775960.4:p.Pro1219_Phe1220insLeuPro
NR_104603.1:n.2765_2770dup
XM_005251934.1:c.2655_2660dup	XP_005251991.1:p.Pro887_Phe888insLeuPro
XM_011518556.1:c.3624_3629dup	XP_011516858.1:p.Pro1210_Phe1211insLeuPro
XM_011518557.1:c.3456_3461dup	XP_011516859.1:p.Pro1154_Phe1155insLeuPro
XM_011518558.1:c.3456_3461dup	XP_011516860.1:p.Pro1154_Phe1155insLeuPro
XM_005251934.3:c.2655_2660dup	XP_005251991.1:p.Pro887_Phe888insLeuPro
XM_011518556.3:c.3624_3629dup	XP_011516858.1:p.Pro1210_Phe1211insLeuPro
XM_011518557.3:c.3456_3461dup	XP_011516859.1:p.Pro1154_Phe1155insLeuPro
XM_011518558.3:c.3456_3461dup	XP_011516860.1:p.Pro1154_Phe1155insLeuPro
NM_173689.7:c.3651_3656dup MANE Select	NP_775960.4:p.Pro1219_Phe1220insLeuPro
NR_104603.2:n.2765_2770dup