Canonical Allele Identifier: CA1877946686

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376991C= , CM000671.2:g.123376991C=	GRCh38
NC_000009.11:g.126139270C= , CM000671.1:g.126139270C=	GRCh37
NC_000009.10:g.125179091C=	NCBI36
NG_051311.1:g.27927C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3787C= MANE Select	ENSP00000362734.3:p.Gln1263=
ENST00000373631.7:c.3787C=	ENSP00000362734.3:p.Gln1263=
ENST00000460253.1:c.2791C=	ENSP00000435279.1:p.Gln931=
NM_173689.6:c.3787C=	NP_775960.4:p.Gln1263=
NR_104603.1:n.2901C=
XM_005251934.1:c.2791C=	XP_005251991.1:p.Gln931=
XM_011518556.1:c.3760C=	XP_011516858.1:p.Gln1254=
XM_011518557.1:c.3592C=	XP_011516859.1:p.Gln1198=
XM_011518558.1:c.3592C=	XP_011516860.1:p.Gln1198=
XM_005251934.3:c.2791C=	XP_005251991.1:p.Gln931=
XM_011518556.3:c.3760C=	XP_011516858.1:p.Gln1254=
XM_011518557.3:c.3592C=	XP_011516859.1:p.Gln1198=
XM_011518558.3:c.3592C=	XP_011516860.1:p.Gln1198=
NM_173689.7:c.3787C= MANE Select	NP_775960.4:p.Gln1263=
NR_104603.2:n.2901C=