Canonical Allele Identifier: CA2428297162

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48523778A= , CM000685.2:g.48523778A=	GRCh38
NC_000023.10:g.48382166A= , CM000685.1:g.48382166A=	GRCh37
NC_000023.9:g.48267110A=	NCBI36
NG_007452.1:g.7003A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000495186.6:c.7A= MANE Select	ENSP00000417052.1:p.Thr3=
ENST00000651615.1:c.7A=	ENSP00000498524.1:p.Thr3=
ENST00000276096.10:n.110-145A=
ENST00000414061.1:c.7A=	ENSP00000405832.1:p.Thr3=
ENST00000446158.5:c.7A=	ENSP00000390031.1:p.Thr3=
ENST00000495186.5:c.7A=	ENSP00000417052.1:p.Thr3=
ENST00000498425.1:n.128A=
NM_006579.2:c.7A=	NP_006570.1:p.Thr3=
NM_006579.3:c.7A= MANE Select	NP_006570.1:p.Thr3=