Canonical Allele Identifier: CA2428298317

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527261A= , CM000685.2:g.48527261A=	GRCh38
NC_000023.10:g.48385649A= , CM000685.1:g.48385649A=	GRCh37
NC_000023.9:g.48270593A=	NCBI36
NG_007452.1:g.10486A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.445A= MANE Select	ENSP00000417052.1:p.Ile149=
ENST00000651615.1:c.445A=	ENSP00000498524.1:p.Ile149=
ENST00000276096.10:n.403A=
ENST00000446158.5:c.445A=	ENSP00000390031.1:p.Ile149=
ENST00000466461.1:n.284A=
ENST00000495186.5:c.445A=	ENSP00000417052.1:p.Ile149=
ENST00000498425.1:n.566A=
NM_006579.2:c.445A=	NP_006570.1:p.Ile149=
NM_006579.3:c.445A= MANE Select	NP_006570.1:p.Ile149=