Canonical Allele Identifier: CA2428298349
Gene: EBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48527347A= , CM000685.2:g.48527347A= GRCh38
NC_000023.10:g.48385735A= , CM000685.1:g.48385735A= GRCh37
NC_000023.9:g.48270679A= NCBI36
NG_007452.1:g.10572A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.469+62A= MANE Select ENSP00000417052.1:n.469+62A=
ENST00000651615.1:c.469+62A= ENSP00000498524.1:n.469+62A=
ENST00000276096.10:n.427+62A=
ENST00000446158.5:c.469+62A= ENSP00000390031.1:n.469+62A=
ENST00000466461.1:n.370A=
ENST00000495186.5:c.469+62A= ENSP00000417052.1:n.469+62A=
ENST00000498425.1:n.590+62A=
NM_006579.2:c.469+62A= NP_006570.1:n.469+62A=
NM_006579.3:c.469+62A= MANE Select NP_006570.1:n.469+62A=
Search 100 bp 5'
Search 100 bp 3'