Canonical Allele Identifier: CA2581927447
Gene: EPHB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.134796494T>C , CM000665.2:g.134796494T>C GRCh38
NC_000003.11:g.134515336T>C , CM000665.1:g.134515336T>C GRCh37
NC_000003.10:g.135998026T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398015.8:c.58+805T>C MANE Select ENSP00000381097.3:n.58+805T>C
ENST00000647596.1:c.58+805T>C ENSP00000497153.1:n.58+805T>C
ENST00000398015.7:c.58+805T>C ENSP00000381097.3:n.58+805T>C
ENST00000460895.5:c.-9+16613T>C ENSP00000417435.1:n.-9+16613T>C
ENST00000482618.5:c.58+805T>C ENSP00000420338.1:n.58+805T>C
ENST00000488154.5:n.58+805T>C
ENST00000497173.5:c.-9+101T>C ENSP00000419688.1:n.-9+101T>C
NM_004441.4:c.58+805T>C NP_004432.1:n.58+805T>C
XM_017005866.2:c.58+805T>C XP_016861355.1:n.58+805T>C
XM_024453389.1:c.-9+16613T>C XP_024309157.1:n.-9+16613T>C
XM_024453390.1:c.-9+16613T>C XP_024309158.1:n.-9+16613T>C
NM_004441.5:c.58+805T>C MANE Select NP_004432.1:n.58+805T>C