Canonical Allele Identifier: CA1877946841

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377071G= , CM000671.2:g.123377071G=	GRCh38
NC_000009.11:g.126139350G= , CM000671.1:g.126139350G=	GRCh37
NC_000009.10:g.125179171G=	NCBI36
NG_051311.1:g.28007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.*9G= MANE Select	ENSP00000362734.3:n.*9G=
ENST00000373631.7:c.*9G=	ENSP00000362734.3:n.*9G=
ENST00000460253.1:c.*9G=	ENSP00000435279.1:n.*9G=
NM_173689.6:c.*9G=	NP_775960.4:n.*9G=
NR_104603.1:n.2981G=
XM_005251934.1:c.*9G=	XP_005251991.1:n.*9G=
XM_011518556.1:c.*9G=	XP_011516858.1:n.*9G=
XM_011518557.1:c.*9G=	XP_011516859.1:n.*9G=
XM_011518558.1:c.*9G=	XP_011516860.1:n.*9G=
XM_005251934.3:c.*9G=	XP_005251991.1:n.*9G=
XM_011518556.3:c.*9G=	XP_011516858.1:n.*9G=
XM_011518557.3:c.*9G=	XP_011516859.1:n.*9G=
XM_011518558.3:c.*9G=	XP_011516860.1:n.*9G=
NM_173689.7:c.*9G= MANE Select	NP_775960.4:n.*9G=
NR_104603.2:n.2981G=