Canonical Allele Identifier: CA1877946884

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377096T= , CM000671.2:g.123377096T=	GRCh38
NC_000009.11:g.126139375T= , CM000671.1:g.126139375T=	GRCh37
NC_000009.10:g.125179196T=	NCBI36
NG_051311.1:g.28032T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.*34T= MANE Select	ENSP00000362734.3:n.*34T=
ENST00000373631.7:c.*34T=	ENSP00000362734.3:n.*34T=
ENST00000460253.1:c.*34T=	ENSP00000435279.1:n.*34T=
NM_173689.6:c.*34T=	NP_775960.4:n.*34T=
NR_104603.1:n.3006T=
XM_005251934.1:c.*34T=	XP_005251991.1:n.*34T=
XM_011518556.1:c.*34T=	XP_011516858.1:n.*34T=
XM_011518557.1:c.*34T=	XP_011516859.1:n.*34T=
XM_011518558.1:c.*34T=	XP_011516860.1:n.*34T=
XM_005251934.3:c.*34T=	XP_005251991.1:n.*34T=
XM_011518556.3:c.*34T=	XP_011516858.1:n.*34T=
XM_011518557.3:c.*34T=	XP_011516859.1:n.*34T=
XM_011518558.3:c.*34T=	XP_011516860.1:n.*34T=
NM_173689.7:c.*34T= MANE Select	NP_775960.4:n.*34T=
NR_104603.2:n.3006T=