Canonical Allele Identifier: CA1877938656

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123373436A= , CM000671.2:g.123373436A=	GRCh38
NC_000009.11:g.126135715A= , CM000671.1:g.126135715A=	GRCh37
NC_000009.10:g.125175536A=	NCBI36
NG_051311.1:g.24372A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.2905A= MANE Select	ENSP00000362734.3:p.Thr969=
ENST00000359999.7:c.2905A=	ENSP00000353092.3:p.Thr969=
ENST00000373631.7:c.2905A=	ENSP00000362734.3:p.Thr969=
ENST00000460253.1:c.1909A=	ENSP00000435279.1:p.Thr637=
NM_173689.6:c.2905A=	NP_775960.4:p.Thr969=
NR_104603.1:n.2019A=
XM_005251934.1:c.1909A=	XP_005251991.1:p.Thr637=
XM_011518556.1:c.2878A=	XP_011516858.1:p.Thr960=
XM_011518557.1:c.2710A=	XP_011516859.1:p.Thr904=
XM_011518558.1:c.2710A=	XP_011516860.1:p.Thr904=
XM_005251934.3:c.1909A=	XP_005251991.1:p.Thr637=
XM_011518556.3:c.2878A=	XP_011516858.1:p.Thr960=
XM_011518557.3:c.2710A=	XP_011516859.1:p.Thr904=
XM_011518558.3:c.2710A=	XP_011516860.1:p.Thr904=
NM_173689.7:c.2905A= MANE Select	NP_775960.4:p.Thr969=
NR_104603.2:n.2019A=