Canonical Allele Identifier: CA1140186384

Gene: EPHB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22807725G= , CM000663.2:g.22807725G=	GRCh38
NC_000001.10:g.23134218G= , CM000663.1:g.23134218G=	GRCh37
NC_000001.9:g.23006805G=	NCBI36
NG_011804.2:g.101888G= , LRG_780:g.101888G=

Transcript Alleles

HGVS	Amino-acid Change
NM_017449.5:c.811+22649G= MANE Select	NP_059145.2:n.811+22649G=
ENST00000374630.8:c.811+22649G= MANE Select	ENSP00000363761.3:n.811+22649G=
NM_001309192.1:c.811+22649G=	NP_001296121.1:n.811+22649G=
NM_001309192.2:c.811+22649G=	NP_001296121.1:n.811+22649G=
NM_001309193.1:c.811+22649G=	NP_001296122.1:n.811+22649G=
NM_001309193.2:c.811+22649G=	NP_001296122.1:n.811+22649G=
NM_004442.6:c.811+22649G=	NP_004433.2:n.811+22649G=
NM_004442.7:c.811+22649G= , LRG_780t1:c.811+22649G=	NP_004433.2:n.811+22649G=
NM_017449.3:c.811+22649G=	NP_059145.2:n.811+22649G=
NM_017449.4:c.811+22649G= , LRG_780t2:c.811+22649G=	NP_059145.2:n.811+22649G=
ENST00000374627.1:c.793+22649G=	ENSP00000363758.1:n.793+22649G=
ENST00000374630.7:c.811+22649G=	ENSP00000363761.3:n.811+22649G=
ENST00000374632.7:c.811+22649G=	ENSP00000363763.3:n.811+22649G=
ENST00000400191.7:c.811+22649G=	ENSP00000383053.3:n.811+22649G=
ENST00000465676.1:n.52+7434G=
ENST00000544305.5:c.811+22649G=	ENSP00000444174.1:n.811+22649G=
XM_006710441.2:c.790+22649G=	XP_006710504.1:n.790+22649G=
XM_006710441.4:c.790+22649G=	XP_006710504.1:n.790+22649G=
XM_006710442.2:c.811+22649G=	XP_006710505.1:n.811+22649G=
XM_006710442.4:c.811+22649G=	XP_006710505.1:n.811+22649G=