Canonical Allele Identifier: CA1140495537

Gene: EPHB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22906853G= , CM000663.2:g.22906853G=	GRCh38
NC_000001.10:g.23233346G= , CM000663.1:g.23233346G=	GRCh37
NC_000001.9:g.23105933G=	NCBI36
NG_011804.2:g.201016G= , LRG_780:g.201016G=

Transcript Alleles

HGVS	Amino-acid Change
NM_017449.5:c.2032G= MANE Select	NP_059145.2:p.Asp678=
ENST00000374630.8:c.2032G= MANE Select	ENSP00000363761.3:p.Asp678=
NM_001309192.1:c.1858G=	NP_001296121.1:p.Asp620=
NM_001309192.2:c.1858G=	NP_001296121.1:p.Asp620=
NM_001309193.1:c.2032G=	NP_001296122.1:p.Asp678=
NM_001309193.2:c.2032G=	NP_001296122.1:p.Asp678=
NM_004442.6:c.2035G=	NP_004433.2:p.Asp679=
NM_004442.7:c.2035G= , LRG_780t1:c.2035G=	NP_004433.2:p.Asp679=
NM_017449.3:c.2032G=	NP_059145.2:p.Asp678=
NM_017449.4:c.2032G= , LRG_780t2:c.2032G=	NP_059145.2:p.Asp678=
ENST00000374627.1:c.2017G=	ENSP00000363758.1:p.Asp673=
ENST00000374630.7:c.2032G=	ENSP00000363761.3:p.Asp678=
ENST00000374632.7:c.2035G=	ENSP00000363763.3:p.Asp679=
ENST00000400191.7:c.2032G=	ENSP00000383053.3:p.Asp678=
XM_006710441.2:c.2014G=	XP_006710504.1:p.Asp672=
XM_006710441.4:c.2014G=	XP_006710504.1:p.Asp672=
XM_006710442.2:c.1942G=	XP_006710505.1:p.Asp648=
XM_006710442.4:c.1942G=	XP_006710505.1:p.Asp648=
XM_011540976.1:c.709G=	XP_011539278.1:p.Asp237=
XM_024453895.1:c.709G=	XP_024309663.1:p.Asp237=