Canonical Allele Identifier: CA1877945933

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376702C= , CM000671.2:g.123376702C=	GRCh38
NC_000009.11:g.126138981C= , CM000671.1:g.126138981C=	GRCh37
NC_000009.10:g.125178802C=	NCBI36
NG_051311.1:g.27638C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3634-136C= MANE Select	ENSP00000362734.3:n.3634-136C=
ENST00000373631.7:c.3634-136C=	ENSP00000362734.3:n.3634-136C=
ENST00000460253.1:c.2638-136C=	ENSP00000435279.1:n.2638-136C=
NM_173689.6:c.3634-136C=	NP_775960.4:n.3634-136C=
NR_104603.1:n.2748-136C=
XM_005251934.1:c.2638-136C=	XP_005251991.1:n.2638-136C=
XM_011518556.1:c.3607-136C=	XP_011516858.1:n.3607-136C=
XM_011518557.1:c.3439-136C=	XP_011516859.1:n.3439-136C=
XM_011518558.1:c.3439-136C=	XP_011516860.1:n.3439-136C=
XM_005251934.3:c.2638-136C=	XP_005251991.1:n.2638-136C=
XM_011518556.3:c.3607-136C=	XP_011516858.1:n.3607-136C=
XM_011518557.3:c.3439-136C=	XP_011516859.1:n.3439-136C=
XM_011518558.3:c.3439-136C=	XP_011516860.1:n.3439-136C=
NM_173689.7:c.3634-136C= MANE Select	NP_775960.4:n.3634-136C=
NR_104603.2:n.2748-136C=