Canonical Allele Identifier: CA1877939751

Gene: CRB2

Linked Data

• dbSNP Id: rs752999904

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123373784_123373798del , CM000671.2:g.123373784_123373798del	GRCh38
NC_000009.11:g.126136063_126136077del , CM000671.1:g.126136063_126136077del	GRCh37
NC_000009.10:g.125175884_125175898del	NCBI36
NG_051311.1:g.24720_24734del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3253_3267del MANE Select	ENSP00000362734.3:p.Gly1085_Pro1089del
ENST00000359999.7:c.3253_3267del	ENSP00000353092.3:p.Gly1085_Pro1089del
ENST00000373631.7:c.3253_3267del	ENSP00000362734.3:p.Gly1085_Pro1089del
ENST00000460253.1:c.2257_2271del	ENSP00000435279.1:p.Gly753_Pro757del
NM_173689.6:c.3253_3267del	NP_775960.4:p.Gly1085_Pro1089del
NR_104603.1:n.2367_2381del
XM_005251934.1:c.2257_2271del	XP_005251991.1:p.Gly753_Pro757del
XM_011518556.1:c.3226_3240del	XP_011516858.1:p.Gly1076_Pro1080del
XM_011518557.1:c.3058_3072del	XP_011516859.1:p.Gly1020_Pro1024del
XM_011518558.1:c.3058_3072del	XP_011516860.1:p.Gly1020_Pro1024del
XM_005251934.3:c.2257_2271del	XP_005251991.1:p.Gly753_Pro757del
XM_011518556.3:c.3226_3240del	XP_011516858.1:p.Gly1076_Pro1080del
XM_011518557.3:c.3058_3072del	XP_011516859.1:p.Gly1020_Pro1024del
XM_011518558.3:c.3058_3072del	XP_011516860.1:p.Gly1020_Pro1024del
NM_173689.7:c.3253_3267del MANE Select	NP_775960.4:p.Gly1085_Pro1089del
NR_104603.2:n.2367_2381del