Canonical Allele Identifier: CA1140013814

Gene: EPHB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22737437T= , CM000663.2:g.22737437T=	GRCh38
NC_000001.10:g.23063930T= , CM000663.1:g.23063930T=	GRCh37
NC_000001.9:g.22936517T=	NCBI36
NG_011804.2:g.31600T= , LRG_780:g.31600T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374630.8:c.61+26394T= MANE Select	ENSP00000363761.3:n.61+26394T=
ENST00000374630.7:c.61+26394T=	ENSP00000363761.3:n.61+26394T=
ENST00000374632.7:c.61+26394T=	ENSP00000363763.3:n.61+26394T=
ENST00000400191.7:c.61+26394T=	ENSP00000383053.3:n.61+26394T=
ENST00000544305.5:c.61+26394T=	ENSP00000444174.1:n.61+26394T=
NM_001309192.1:c.61+26394T=	NP_001296121.1:n.61+26394T=
NM_001309193.1:c.61+26394T=	NP_001296122.1:n.61+26394T=
NM_004442.6:c.61+26394T=	NP_004433.2:n.61+26394T=
NM_004442.7:c.61+26394T= , LRG_780t1:c.61+26394T=	NP_004433.2:n.61+26394T=
NM_017449.3:c.61+26394T=	NP_059145.2:n.61+26394T=
NM_017449.4:c.61+26394T= , LRG_780t2:c.61+26394T=	NP_059145.2:n.61+26394T=
XM_006710442.2:c.61+26394T=	XP_006710505.1:n.61+26394T=
XM_006710442.4:c.61+26394T=	XP_006710505.1:n.61+26394T=
NM_001309192.2:c.61+26394T=	NP_001296121.1:n.61+26394T=
NM_001309193.2:c.61+26394T=	NP_001296122.1:n.61+26394T=
NM_017449.5:c.61+26394T= MANE Select	NP_059145.2:n.61+26394T=