Canonical Allele Identifier: CA1877946668

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376980G= , CM000671.2:g.123376980G=	GRCh38
NC_000009.11:g.126139259G= , CM000671.1:g.126139259G=	GRCh37
NC_000009.10:g.125179080G=	NCBI36
NG_051311.1:g.27916G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3776G= MANE Select	ENSP00000362734.3:p.Ser1259=
ENST00000373631.7:c.3776G=	ENSP00000362734.3:p.Ser1259=
ENST00000460253.1:c.2780G=	ENSP00000435279.1:p.Ser927=
NM_173689.6:c.3776G=	NP_775960.4:p.Ser1259=
NR_104603.1:n.2890G=
XM_005251934.1:c.2780G=	XP_005251991.1:p.Ser927=
XM_011518556.1:c.3749G=	XP_011516858.1:p.Ser1250=
XM_011518557.1:c.3581G=	XP_011516859.1:p.Ser1194=
XM_011518558.1:c.3581G=	XP_011516860.1:p.Ser1194=
XM_005251934.3:c.2780G=	XP_005251991.1:p.Ser927=
XM_011518556.3:c.3749G=	XP_011516858.1:p.Ser1250=
XM_011518557.3:c.3581G=	XP_011516859.1:p.Ser1194=
XM_011518558.3:c.3581G=	XP_011516860.1:p.Ser1194=
NM_173689.7:c.3776G= MANE Select	NP_775960.4:p.Ser1259=
NR_104603.2:n.2890G=