Canonical Allele Identifier: CA2428298333
Gene: EBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48527312T= , CM000685.2:g.48527312T= GRCh38
NC_000023.10:g.48385700T= , CM000685.1:g.48385700T= GRCh37
NC_000023.9:g.48270644T= NCBI36
NG_007452.1:g.10537T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.469+27T= MANE Select ENSP00000417052.1:n.469+27T=
ENST00000651615.1:c.469+27T= ENSP00000498524.1:n.469+27T=
ENST00000276096.10:n.427+27T=
ENST00000446158.5:c.469+27T= ENSP00000390031.1:n.469+27T=
ENST00000466461.1:n.335T=
ENST00000495186.5:c.469+27T= ENSP00000417052.1:n.469+27T=
ENST00000498425.1:n.590+27T=
NM_006579.2:c.469+27T= NP_006570.1:n.469+27T=
NM_006579.3:c.469+27T= MANE Select NP_006570.1:n.469+27T=
Search 100 bp 5'
Search 100 bp 3'