Canonical Allele Identifier: CA2428298600
Gene: EBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528207T= , CM000685.2:g.48528207T= GRCh38
NC_000023.10:g.48386595T= , CM000685.1:g.48386595T= GRCh37
NC_000023.9:g.48271539T= NCBI36
NG_007452.1:g.11432T=

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.470-27T= MANE Select ENSP00000417052.1:n.470-27T=
ENST00000651615.1:c.469+922T= ENSP00000498524.1:n.469+922T=
ENST00000276096.10:n.428-27T=
ENST00000446158.5:c.470-27T= ENSP00000390031.1:n.470-27T=
ENST00000495186.5:c.470-27T= ENSP00000417052.1:n.470-27T=
ENST00000498425.1:n.591-27T=
NM_006579.2:c.470-27T= NP_006570.1:n.470-27T=
NM_006579.3:c.470-27T= MANE Select NP_006570.1:n.470-27T=