Canonical Allele Identifier: CA2428298591
Gene: EBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528189C= , CM000685.2:g.48528189C= GRCh38
NC_000023.10:g.48386577C= , CM000685.1:g.48386577C= GRCh37
NC_000023.9:g.48271521C= NCBI36
NG_007452.1:g.11414C=

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.470-45C= MANE Select ENSP00000417052.1:n.470-45C=
ENST00000651615.1:c.469+904C= ENSP00000498524.1:n.469+904C=
ENST00000276096.10:n.428-45C=
ENST00000446158.5:c.470-45C= ENSP00000390031.1:n.470-45C=
ENST00000495186.5:c.470-45C= ENSP00000417052.1:n.470-45C=
ENST00000498425.1:n.591-45C=
NM_006579.2:c.470-45C= NP_006570.1:n.470-45C=
NM_006579.3:c.470-45C= MANE Select NP_006570.1:n.470-45C=