Canonical Allele Identifier: CA1877939839

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123373797C= , CM000671.2:g.123373797C=	GRCh38
NC_000009.11:g.126136076C= , CM000671.1:g.126136076C=	GRCh37
NC_000009.10:g.125175897C=	NCBI36
NG_051311.1:g.24733C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373631.8:c.3266C= MANE Select	ENSP00000362734.3:p.Pro1089=
ENST00000359999.7:c.3266C=	ENSP00000353092.3:p.Pro1089=
ENST00000373631.7:c.3266C=	ENSP00000362734.3:p.Pro1089=
ENST00000460253.1:c.2270C=	ENSP00000435279.1:p.Pro757=
NM_173689.6:c.3266C=	NP_775960.4:p.Pro1089=
NR_104603.1:n.2380C=
XM_005251934.1:c.2270C=	XP_005251991.1:p.Pro757=
XM_011518556.1:c.3239C=	XP_011516858.1:p.Pro1080=
XM_011518557.1:c.3071C=	XP_011516859.1:p.Pro1024=
XM_011518558.1:c.3071C=	XP_011516860.1:p.Pro1024=
XM_005251934.3:c.2270C=	XP_005251991.1:p.Pro757=
XM_011518556.3:c.3239C=	XP_011516858.1:p.Pro1080=
XM_011518557.3:c.3071C=	XP_011516859.1:p.Pro1024=
XM_011518558.3:c.3071C=	XP_011516860.1:p.Pro1024=
NM_173689.7:c.3266C= MANE Select	NP_775960.4:p.Pro1089=
NR_104603.2:n.2380C=