Canonical Allele Identifier: CA1877946726

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377012C= , CM000671.2:g.123377012C=	GRCh38
NC_000009.11:g.126139291C= , CM000671.1:g.126139291C=	GRCh37
NC_000009.10:g.125179112C=	NCBI36
NG_051311.1:g.27948C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3808C= MANE Select	ENSP00000362734.3:p.Leu1270=
ENST00000373631.7:c.3808C=	ENSP00000362734.3:p.Leu1270=
ENST00000460253.1:c.2812C=	ENSP00000435279.1:p.Leu938=
NM_173689.6:c.3808C=	NP_775960.4:p.Leu1270=
NR_104603.1:n.2922C=
XM_005251934.1:c.2812C=	XP_005251991.1:p.Leu938=
XM_011518556.1:c.3781C=	XP_011516858.1:p.Leu1261=
XM_011518557.1:c.3613C=	XP_011516859.1:p.Leu1205=
XM_011518558.1:c.3613C=	XP_011516860.1:p.Leu1205=
XM_005251934.3:c.2812C=	XP_005251991.1:p.Leu938=
XM_011518556.3:c.3781C=	XP_011516858.1:p.Leu1261=
XM_011518557.3:c.3613C=	XP_011516859.1:p.Leu1205=
XM_011518558.3:c.3613C=	XP_011516860.1:p.Leu1205=
NM_173689.7:c.3808C= MANE Select	NP_775960.4:p.Leu1270=
NR_104603.2:n.2922C=