Canonical Allele Identifier: CA10719150
Gene: EPHB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22740551G>A , CM000663.2:g.22740551G>A GRCh38
NC_000001.10:g.23067044G>A , CM000663.1:g.23067044G>A GRCh37
NC_000001.9:g.22939631G>A NCBI36
NG_011804.2:g.34714G>A , LRG_780:g.34714G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374630.8:c.61+29508G>A MANE Select ENSP00000363761.3:n.61+29508G>A
ENST00000374630.7:c.61+29508G>A ENSP00000363761.3:n.61+29508G>A
ENST00000374632.7:c.61+29508G>A ENSP00000363763.3:n.61+29508G>A
ENST00000400191.7:c.61+29508G>A ENSP00000383053.3:n.61+29508G>A
ENST00000544305.5:c.61+29508G>A ENSP00000444174.1:n.61+29508G>A
NM_001309192.1:c.61+29508G>A NP_001296121.1:n.61+29508G>A
NM_001309193.1:c.61+29508G>A NP_001296122.1:n.61+29508G>A
NM_004442.6:c.61+29508G>A NP_004433.2:n.61+29508G>A
NM_004442.7:c.61+29508G>A , LRG_780t1:c.61+29508G>A NP_004433.2:n.61+29508G>A
NM_017449.3:c.61+29508G>A NP_059145.2:n.61+29508G>A
NM_017449.4:c.61+29508G>A , LRG_780t2:c.61+29508G>A NP_059145.2:n.61+29508G>A
XM_006710442.2:c.61+29508G>A XP_006710505.1:n.61+29508G>A
XM_006710442.4:c.61+29508G>A XP_006710505.1:n.61+29508G>A
NM_001309192.2:c.61+29508G>A NP_001296121.1:n.61+29508G>A
NM_001309193.2:c.61+29508G>A NP_001296122.1:n.61+29508G>A
NM_017449.5:c.61+29508G>A MANE Select NP_059145.2:n.61+29508G>A
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