Canonical Allele Identifier: CA1877946411

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376883G= , CM000671.2:g.123376883G=	GRCh38
NC_000009.11:g.126139162G= , CM000671.1:g.126139162G=	GRCh37
NC_000009.10:g.125178983G=	NCBI36
NG_051311.1:g.27819G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3679G= MANE Select	ENSP00000362734.3:p.Val1227=
ENST00000373631.7:c.3679G=	ENSP00000362734.3:p.Val1227=
ENST00000460253.1:c.2683G=	ENSP00000435279.1:p.Val895=
NM_173689.6:c.3679G=	NP_775960.4:p.Val1227=
NR_104603.1:n.2793G=
XM_005251934.1:c.2683G=	XP_005251991.1:p.Val895=
XM_011518556.1:c.3652G=	XP_011516858.1:p.Val1218=
XM_011518557.1:c.3484G=	XP_011516859.1:p.Val1162=
XM_011518558.1:c.3484G=	XP_011516860.1:p.Val1162=
XM_005251934.3:c.2683G=	XP_005251991.1:p.Val895=
XM_011518556.3:c.3652G=	XP_011516858.1:p.Val1218=
XM_011518557.3:c.3484G=	XP_011516859.1:p.Val1162=
XM_011518558.3:c.3484G=	XP_011516860.1:p.Val1162=
NM_173689.7:c.3679G= MANE Select	NP_775960.4:p.Val1227=
NR_104603.2:n.2793G=