Canonical Allele Identifier: CA2428298579
Gene: EBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528157A= , CM000685.2:g.48528157A= GRCh38
NC_000023.10:g.48386545A= , CM000685.1:g.48386545A= GRCh37
NC_000023.9:g.48271489A= NCBI36
NG_007452.1:g.11382A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.470-77A= MANE Select ENSP00000417052.1:n.470-77A=
ENST00000651615.1:c.469+872A= ENSP00000498524.1:n.469+872A=
ENST00000276096.10:n.428-77A=
ENST00000446158.5:c.470-77A= ENSP00000390031.1:n.470-77A=
ENST00000495186.5:c.470-77A= ENSP00000417052.1:n.470-77A=
ENST00000498425.1:n.591-77A=
NM_006579.2:c.470-77A= NP_006570.1:n.470-77A=
NM_006579.3:c.470-77A= MANE Select NP_006570.1:n.470-77A=