Canonical Allele Identifier: CA2428298586
Gene: EBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528183A= , CM000685.2:g.48528183A= GRCh38
NC_000023.10:g.48386571A= , CM000685.1:g.48386571A= GRCh37
NC_000023.9:g.48271515A= NCBI36
NG_007452.1:g.11408A=

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.470-51A= MANE Select ENSP00000417052.1:n.470-51A=
ENST00000651615.1:c.469+898A= ENSP00000498524.1:n.469+898A=
ENST00000276096.10:n.428-51A=
ENST00000446158.5:c.470-51A= ENSP00000390031.1:n.470-51A=
ENST00000495186.5:c.470-51A= ENSP00000417052.1:n.470-51A=
ENST00000498425.1:n.591-51A=
NM_006579.2:c.470-51A= NP_006570.1:n.470-51A=
NM_006579.3:c.470-51A= MANE Select NP_006570.1:n.470-51A=