Canonical Allele Identifier: CA1877945628

Gene: CRB2

Linked Data

• dbSNP Id: rs2042105635

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376525_123376526insT , CM000671.2:g.123376525_123376526insT	GRCh38
NC_000009.11:g.126138804_126138805insT , CM000671.1:g.126138804_126138805insT	GRCh37
NC_000009.10:g.125178625_125178626insT	NCBI36
NG_051311.1:g.27461_27462insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3634-313_3634-312insT MANE Select	ENSP00000362734.3:n.3634-313_3634-312insT
ENST00000373631.7:c.3634-313_3634-312insT	ENSP00000362734.3:n.3634-313_3634-312insT
ENST00000460253.1:c.2638-313_2638-312insT	ENSP00000435279.1:n.2638-313_2638-312insT
NM_173689.6:c.3634-313_3634-312insT	NP_775960.4:n.3634-313_3634-312insT
NR_104603.1:n.2748-313_2748-312insT
XM_005251934.1:c.2638-313_2638-312insT	XP_005251991.1:n.2638-313_2638-312insT
XM_011518556.1:c.3607-313_3607-312insT	XP_011516858.1:n.3607-313_3607-312insT
XM_011518557.1:c.3439-313_3439-312insT	XP_011516859.1:n.3439-313_3439-312insT
XM_011518558.1:c.3439-313_3439-312insT	XP_011516860.1:n.3439-313_3439-312insT
XM_005251934.3:c.2638-313_2638-312insT	XP_005251991.1:n.2638-313_2638-312insT
XM_011518556.3:c.3607-313_3607-312insT	XP_011516858.1:n.3607-313_3607-312insT
XM_011518557.3:c.3439-313_3439-312insT	XP_011516859.1:n.3439-313_3439-312insT
XM_011518558.3:c.3439-313_3439-312insT	XP_011516860.1:n.3439-313_3439-312insT
NM_173689.7:c.3634-313_3634-312insT MANE Select	NP_775960.4:n.3634-313_3634-312insT
NR_104603.2:n.2748-313_2748-312insT