Canonical Allele Identifier: CA12108339
Gene: EBF1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10040979

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.158997383G>A , CM000667.2:g.158997383G>A GRCh38
NC_000005.9:g.158424391G>A , CM000667.1:g.158424391G>A GRCh37
NC_000005.8:g.158356969G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001290360.1:c.554+76013C>T VV NP_001277289.1:p.=
NM_024007.3:c.554+76013C>T VV NP_076870.1:p.=
NM_182708.1:c.485+87283C>T VV NP_874367.1:p.=
XM_005265834.1:c.554+76013C>T XP_005265891.1:p.=
XM_011534452.1:c.554+76013C>T XP_011532754.1:p.=
XM_011534453.1:c.554+76013C>T XP_011532755.1:p.=
XM_011534454.1:c.554+76013C>T XP_011532756.1:p.=
XM_011534455.1:c.554+76013C>T XP_011532757.1:p.=
XM_011534456.1:c.440+76013C>T XP_011532758.1:p.=
XM_011534457.1:c.-68+55396C>T XP_011532759.1:p.=
NM_001290360.2:c.554+76013C>T VV
NM_001324101.1:c.554+76013C>T VV NP_001311030.1:p.=
NM_001324103.1:c.554+76013C>T VV NP_001311032.1:p.=
NM_001324106.1:c.554+76013C>T VV NP_001311035.1:p.=
NM_001324107.1:c.554+76013C>T VV NP_001311036.1:p.=
NM_001324108.1:c.554+76013C>T VV NP_001311037.1:p.=
NM_001324109.1:c.554+76013C>T VV NP_001311038.1:p.=
NM_001324111.1:c.155+76013C>T VV NP_001311040.1:p.=
NM_001364155.1:c.554+76013C>T VV NP_001351084.1:p.=
NM_001364156.1:c.440+76013C>T VV NP_001351085.1:p.=
NM_001364157.1:c.440+76013C>T VV NP_001351086.1:p.=
NM_001364158.1:c.155+76013C>T VV NP_001351087.1:p.=
NM_001364159.1:c.155+76013C>T VV NP_001351088.1:p.=
NM_024007.4:c.554+76013C>T VV
NM_182708.2:c.485+87283C>T VV
XM_017009192.1:c.554+76013C>T XP_016864681.1:p.=
XM_017009193.1:c.554+76013C>T XP_016864682.1:p.=
XM_017009194.1:c.554+76013C>T XP_016864683.1:p.=
XM_017009195.1:c.554+76013C>T XP_016864684.1:p.=
XM_017009196.1:c.440+76013C>T XP_016864685.1:p.=
XM_017009197.1:c.440+76013C>T XP_016864686.1:p.=
XM_017009200.2:c.-68+55396C>T XP_016864689.1:p.=
XM_017009201.2:c.-68+55396C>T XP_016864690.1:p.=
XM_017009202.1:c.554+76013C>T XP_016864691.1:p.=
XM_017009203.1:c.554+76013C>T XP_016864692.1:p.=
XM_024454390.1:c.155+76013C>T XP_024310158.1:p.=
XM_024454391.1:c.155+76013C>T XP_024310159.1:p.=
XM_024454392.1:c.155+76013C>T XP_024310160.1:p.=
XM_024454393.1:c.155+76013C>T XP_024310161.1:p.=
ENST00000313708.10:c.554+76013C>T ENSP00000322898.6:p.=
ENST00000380654.8:c.485+87283C>T ENSP00000370029.4:p.=
ENST00000517373.1:c.554+76013C>T ENSP00000428020.1:p.=
ENST00000518836.5:n.714+76013C>T
ENST00000519739.5:n.322+76013C>T
ENST00000519890.5:n.282+76013C>T
ENST00000522192.5:n.463+76013C>T
ENST00000523464.1:n.170+21577C>T