Canonical Allele Identifier: CA1729513850
Gene: EPHB4 HGNC NCBI

Linked Data

dbSNP Id: rs314313
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100825743T>G , CM000669.2:g.100825743T>G GRCh38
NC_000007.13:g.100423365T>G , CM000669.1:g.100423365T>G GRCh37
NC_000007.12:g.100261301T>G NCBI36
NG_052671.1:g.6779A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358173.8:c.52+1236A>C MANE Select ENSP00000350896.3:n.52+1236A>C
ENST00000358173.7:c.52+1236A>C ENSP00000350896.3:n.52+1236A>C
ENST00000360620.7:c.52+1236A>C ENSP00000353833.3:n.52+1236A>C
ENST00000477446.5:n.52+1236A>C
ENST00000489808.1:n.52+1236A>C
ENST00000616502.4:c.52+1236A>C ENSP00000482702.1:n.52+1236A>C
NM_004444.4:c.52+1236A>C NP_004435.3:n.52+1236A>C
XM_017011816.1:c.52+1236A>C XP_016867305.1:n.52+1236A>C
NM_004444.5:c.52+1236A>C MANE Select NP_004435.3:n.52+1236A>C
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