Canonical Allele Identifier: CA1403803454

Gene: EPHB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.135193075A>T , CM000665.2:g.135193075A>T	GRCh38
NC_000003.11:g.134911917A>T , CM000665.1:g.134911917A>T	GRCh37
NC_000003.10:g.136394607A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398015.8:c.2130+252A>T MANE Select	ENSP00000381097.3:n.2130+252A>T
ENST00000647596.1:c.2130+252A>T	ENSP00000497153.1:n.2130+252A>T
ENST00000398015.7:c.2130+252A>T	ENSP00000381097.3:n.2130+252A>T
ENST00000493838.1:c.813+252A>T	ENSP00000419574.1:n.813+252A>T
NM_004441.4:c.2130+252A>T	NP_004432.1:n.2130+252A>T
XM_011512540.1:c.2112+252A>T	XP_011510842.1:n.2112+252A>T
XM_011512541.1:c.2064+252A>T	XP_011510843.1:n.2064+252A>T
XM_011512542.1:c.360+252A>T	XP_011510844.1:n.360+252A>T
XM_017005866.2:c.2292+252A>T	XP_016861355.1:n.2292+252A>T
XM_017005867.1:c.2274+252A>T	XP_016861356.1:n.2274+252A>T
XM_024453389.1:c.2226+252A>T	XP_024309157.1:n.2226+252A>T
XM_024453390.1:c.2226+252A>T	XP_024309158.1:n.2226+252A>T
NM_004441.5:c.2130+252A>T MANE Select	NP_004432.1:n.2130+252A>T