Canonical Allele Identifier: CA16158799
Gene: EPHB1 HGNC NCBI

Linked Data

dbSNP Id: rs11929692
gnomAD v2: 3-134669965-G-A
gnomAD v3: 3-134951123-G-A
gnomAD v4: 3-134951123-G-A
MyVariant Identifiers: chr3:g.134669965G>A (hg19) chr3:g.134951123G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.134951123G>A , CM000665.2:g.134951123G>A GRCh38
NC_000003.11:g.134669965G>A , CM000665.1:g.134669965G>A GRCh37
NC_000003.10:g.136152655G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398015.8:c.124-248G>A MANE Select ENSP00000381097.3:n.124-248G>A
ENST00000647596.1:c.124-248G>A ENSP00000497153.1:n.124-248G>A
ENST00000398015.7:c.124-248G>A ENSP00000381097.3:n.124-248G>A
ENST00000460895.5:c.58-248G>A ENSP00000417435.1:n.58-248G>A
ENST00000473867.5:c.58-248G>A ENSP00000417216.1:n.58-248G>A
ENST00000474732.1:c.58-248G>A ENSP00000418352.1:n.58-248G>A
ENST00000482618.5:c.124-248G>A ENSP00000420338.1:n.124-248G>A
ENST00000488154.5:n.124-248G>A
ENST00000497173.5:c.58-248G>A ENSP00000419688.1:n.58-248G>A
NM_004441.4:c.124-248G>A NP_004432.1:n.124-248G>A
XM_011512540.1:c.106-248G>A XP_011510842.1:n.106-248G>A
XM_011512541.1:c.58-248G>A XP_011510843.1:n.58-248G>A
XM_017005866.2:c.124-248G>A XP_016861355.1:n.124-248G>A
XM_017005867.1:c.106-248G>A XP_016861356.1:n.106-248G>A
XM_024453389.1:c.58-248G>A XP_024309157.1:n.58-248G>A
XM_024453390.1:c.58-248G>A XP_024309158.1:n.58-248G>A
NM_004441.5:c.124-248G>A MANE Select NP_004432.1:n.124-248G>A
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