Canonical Allele Identifier: CA1140351708

Gene: EPHB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22828738A= , CM000663.2:g.22828738A=	GRCh38
NC_000001.10:g.23155231A= , CM000663.1:g.23155231A=	GRCh37
NC_000001.9:g.23027818A=	NCBI36
NG_011804.2:g.122901A= , LRG_780:g.122901A=

Transcript Alleles

HGVS	Amino-acid Change
NM_017449.5:c.812-34299A= MANE Select	NP_059145.2:n.812-34299A=
ENST00000374630.8:c.812-34299A= MANE Select	ENSP00000363761.3:n.812-34299A=
NM_001309192.1:c.812-34299A=	NP_001296121.1:n.812-34299A=
NM_001309192.2:c.812-34299A=	NP_001296121.1:n.812-34299A=
NM_001309193.1:c.812-34299A=	NP_001296122.1:n.812-34299A=
NM_001309193.2:c.812-34299A=	NP_001296122.1:n.812-34299A=
NM_004442.6:c.812-34299A=	NP_004433.2:n.812-34299A=
NM_004442.7:c.812-34299A= , LRG_780t1:c.812-34299A=	NP_004433.2:n.812-34299A=
NM_017449.3:c.812-34299A=	NP_059145.2:n.812-34299A=
NM_017449.4:c.812-34299A= , LRG_780t2:c.812-34299A=	NP_059145.2:n.812-34299A=
ENST00000374627.1:c.794-34299A=	ENSP00000363758.1:n.794-34299A=
ENST00000374630.7:c.812-34299A=	ENSP00000363761.3:n.812-34299A=
ENST00000374632.7:c.812-34299A=	ENSP00000363763.3:n.812-34299A=
ENST00000400191.7:c.812-34299A=	ENSP00000383053.3:n.812-34299A=
ENST00000465676.1:n.52+28447A=
ENST00000544305.5:c.812-34299A=	ENSP00000444174.1:n.812-34299A=
XM_006710441.2:c.791-34299A=	XP_006710504.1:n.791-34299A=
XM_006710441.4:c.791-34299A=	XP_006710504.1:n.791-34299A=
XM_006710442.2:c.812-34299A=	XP_006710505.1:n.812-34299A=
XM_006710442.4:c.812-34299A=	XP_006710505.1:n.812-34299A=