Canonical Allele Identifier: CA2428297193

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48523868G= , CM000685.2:g.48523868G=	GRCh38
NC_000023.10:g.48382256G= , CM000685.1:g.48382256G=	GRCh37
NC_000023.9:g.48267200G=	NCBI36
NG_007452.1:g.7093G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000495186.6:c.97G= MANE Select	ENSP00000417052.1:p.Ala33=
ENST00000651615.1:c.97G=	ENSP00000498524.1:p.Ala33=
ENST00000276096.10:n.110-55G=
ENST00000414061.1:c.97G=	ENSP00000405832.1:p.Ala33=
ENST00000446158.5:c.97G=	ENSP00000390031.1:p.Ala33=
ENST00000495186.5:c.97G=	ENSP00000417052.1:p.Ala33=
ENST00000498425.1:n.218G=
NM_006579.2:c.97G=	NP_006570.1:p.Ala33=
NM_006579.3:c.97G= MANE Select	NP_006570.1:p.Ala33=