Canonical Allele Identifier: CA1877939823

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123373794G= , CM000671.2:g.123373794G=	GRCh38
NC_000009.11:g.126136073G= , CM000671.1:g.126136073G=	GRCh37
NC_000009.10:g.125175894G=	NCBI36
NG_051311.1:g.24730G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3263G= MANE Select	ENSP00000362734.3:p.Gly1088=
ENST00000359999.7:c.3263G=	ENSP00000353092.3:p.Gly1088=
ENST00000373631.7:c.3263G=	ENSP00000362734.3:p.Gly1088=
ENST00000460253.1:c.2267G=	ENSP00000435279.1:p.Gly756=
NM_173689.6:c.3263G=	NP_775960.4:p.Gly1088=
NR_104603.1:n.2377G=
XM_005251934.1:c.2267G=	XP_005251991.1:p.Gly756=
XM_011518556.1:c.3236G=	XP_011516858.1:p.Gly1079=
XM_011518557.1:c.3068G=	XP_011516859.1:p.Gly1023=
XM_011518558.1:c.3068G=	XP_011516860.1:p.Gly1023=
XM_005251934.3:c.2267G=	XP_005251991.1:p.Gly756=
XM_011518556.3:c.3236G=	XP_011516858.1:p.Gly1079=
XM_011518557.3:c.3068G=	XP_011516859.1:p.Gly1023=
XM_011518558.3:c.3068G=	XP_011516860.1:p.Gly1023=
NM_173689.7:c.3263G= MANE Select	NP_775960.4:p.Gly1088=
NR_104603.2:n.2377G=