Canonical Allele Identifier: CA2428298291

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527184C= , CM000685.2:g.48527184C=	GRCh38
NC_000023.10:g.48385572C= , CM000685.1:g.48385572C=	GRCh37
NC_000023.9:g.48270516C=	NCBI36
NG_007452.1:g.10409C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.368C= MANE Select	ENSP00000417052.1:p.Thr123=
ENST00000651615.1:c.368C=	ENSP00000498524.1:p.Thr123=
ENST00000276096.10:n.326C=
ENST00000414061.1:c.368C=	ENSP00000405832.1:p.Thr123=
ENST00000446158.5:c.368C=	ENSP00000390031.1:p.Thr123=
ENST00000466461.1:n.207C=
ENST00000495186.5:c.368C=	ENSP00000417052.1:p.Thr123=
ENST00000498425.1:n.489C=
NM_006579.2:c.368C=	NP_006570.1:p.Thr123=
NM_006579.3:c.368C= MANE Select	NP_006570.1:p.Thr123=