Canonical Allele Identifier: CA4392809

Gene: EPHB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100813086G>A , CM000669.2:g.100813086G>A	GRCh38
NC_000007.13:g.100410708G>A , CM000669.1:g.100410708G>A	GRCh37
NC_000007.12:g.100248644G>A	NCBI36
NG_052671.1:g.19436C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004444.5:c.1870+9C>T MANE Select	NP_004435.3:n.1870+9C>T
ENST00000358173.8:c.1870+9C>T MANE Select	ENSP00000350896.3:n.1870+9C>T
NM_004444.4:c.1870+9C>T	NP_004435.3:n.1870+9C>T
ENST00000358173.7:c.1870+9C>T	ENSP00000350896.3:n.1870+9C>T
ENST00000360620.7:c.1870+9C>T	ENSP00000353833.3:n.1870+9C>T
ENST00000467515.1:n.245+9C>T
ENST00000478459.5:n.349+9C>T
ENST00000487222.5:n.3071+9C>T
ENST00000616502.4:c.*335+9C>T	ENSP00000482702.1:n.*335+9C>T
XM_017011816.1:c.1924+9C>T	XP_016867305.1:n.1924+9C>T