Canonical Allele Identifier: CA2428297194

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48523870T= , CM000685.2:g.48523870T=	GRCh38
NC_000023.10:g.48382258T= , CM000685.1:g.48382258T=	GRCh37
NC_000023.9:g.48267202T=	NCBI36
NG_007452.1:g.7095T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000495186.6:c.99T= MANE Select	ENSP00000417052.1:p.Ala33=
ENST00000651615.1:c.99T=	ENSP00000498524.1:p.Ala33=
ENST00000276096.10:n.110-53T=
ENST00000414061.1:c.99T=	ENSP00000405832.1:p.Ala33=
ENST00000446158.5:c.99T=	ENSP00000390031.1:p.Ala33=
ENST00000495186.5:c.99T=	ENSP00000417052.1:p.Ala33=
ENST00000498425.1:n.220T=
NM_006579.2:c.99T=	NP_006570.1:p.Ala33=
NM_006579.3:c.99T= MANE Select	NP_006570.1:p.Ala33=