Canonical Allele Identifier: CA1140594661

Gene: EPHB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22863060G= , CM000663.2:g.22863060G=	GRCh38
NC_000001.10:g.23189553G= , CM000663.1:g.23189553G=	GRCh37
NC_000001.9:g.23062140G=	NCBI36
NG_011804.2:g.157223G= , LRG_780:g.157223G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374630.8:c.835G= MANE Select	ENSP00000363761.3:p.Ala279=
ENST00000374627.1:c.817G=	ENSP00000363758.1:p.Ala273=
ENST00000374630.7:c.835G=	ENSP00000363761.3:p.Ala279=
ENST00000374632.7:c.835G=	ENSP00000363763.3:p.Ala279=
ENST00000400191.7:c.835G=	ENSP00000383053.3:p.Ala279=
ENST00000465676.1:n.76G=
ENST00000544305.5:c.835G=	ENSP00000444174.1:p.Ala279=
NM_001309192.1:c.835G=	NP_001296121.1:p.Ala279=
NM_001309193.1:c.835G=	NP_001296122.1:p.Ala279=
NM_004442.6:c.835G=	NP_004433.2:p.Ala279=
NM_004442.7:c.835G= , LRG_780t1:c.835G=	NP_004433.2:p.Ala279=
NM_017449.3:c.835G=	NP_059145.2:p.Ala279=
NM_017449.4:c.835G= , LRG_780t2:c.835G=	NP_059145.2:p.Ala279=
XM_006710441.2:c.814G=	XP_006710504.1:p.Ala272=
XM_006710442.2:c.835G=	XP_006710505.1:p.Ala279=
XM_006710441.4:c.814G=	XP_006710504.1:p.Ala272=
XM_006710442.4:c.835G=	XP_006710505.1:p.Ala279=
NM_001309192.2:c.835G=	NP_001296121.1:p.Ala279=
NM_001309193.2:c.835G=	NP_001296122.1:p.Ala279=
NM_017449.5:c.835G= MANE Select	NP_059145.2:p.Ala279=