Canonical Allele Identifier: CA2428298578
Gene: EBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528153G= , CM000685.2:g.48528153G= GRCh38
NC_000023.10:g.48386541G= , CM000685.1:g.48386541G= GRCh37
NC_000023.9:g.48271485G= NCBI36
NG_007452.1:g.11378G=

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.470-81G= MANE Select ENSP00000417052.1:n.470-81G=
ENST00000651615.1:c.469+868G= ENSP00000498524.1:n.469+868G=
ENST00000276096.10:n.428-81G=
ENST00000446158.5:c.470-81G= ENSP00000390031.1:n.470-81G=
ENST00000495186.5:c.470-81G= ENSP00000417052.1:n.470-81G=
ENST00000498425.1:n.591-81G=
NM_006579.2:c.470-81G= NP_006570.1:n.470-81G=
NM_006579.3:c.470-81G= MANE Select NP_006570.1:n.470-81G=
Search 100 bp 5'
Search 100 bp 3'