Canonical Allele Identifier: CA1877946375

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376869T= , CM000671.2:g.123376869T=	GRCh38
NC_000009.11:g.126139148T= , CM000671.1:g.126139148T=	GRCh37
NC_000009.10:g.125178969T=	NCBI36
NG_051311.1:g.27805T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3665T= MANE Select	ENSP00000362734.3:p.Leu1222=
ENST00000373631.7:c.3665T=	ENSP00000362734.3:p.Leu1222=
ENST00000460253.1:c.2669T=	ENSP00000435279.1:p.Leu890=
NM_173689.6:c.3665T=	NP_775960.4:p.Leu1222=
NR_104603.1:n.2779T=
XM_005251934.1:c.2669T=	XP_005251991.1:p.Leu890=
XM_011518556.1:c.3638T=	XP_011516858.1:p.Leu1213=
XM_011518557.1:c.3470T=	XP_011516859.1:p.Leu1157=
XM_011518558.1:c.3470T=	XP_011516860.1:p.Leu1157=
XM_005251934.3:c.2669T=	XP_005251991.1:p.Leu890=
XM_011518556.3:c.3638T=	XP_011516858.1:p.Leu1213=
XM_011518557.3:c.3470T=	XP_011516859.1:p.Leu1157=
XM_011518558.3:c.3470T=	XP_011516860.1:p.Leu1157=
NM_173689.7:c.3665T= MANE Select	NP_775960.4:p.Leu1222=
NR_104603.2:n.2779T=