Canonical Allele Identifier: CA2579599796
Gene: EBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48527346C>A , CM000685.2:g.48527346C>A GRCh38
NC_000023.10:g.48385734C>A , CM000685.1:g.48385734C>A GRCh37
NC_000023.9:g.48270678C>A NCBI36
NG_007452.1:g.10571C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.469+61C>A MANE Select ENSP00000417052.1:n.469+61C>A
ENST00000651615.1:c.469+61C>A ENSP00000498524.1:n.469+61C>A
ENST00000276096.10:n.427+61C>A
ENST00000446158.5:c.469+61C>A ENSP00000390031.1:n.469+61C>A
ENST00000466461.1:n.369C>A
ENST00000495186.5:c.469+61C>A ENSP00000417052.1:n.469+61C>A
ENST00000498425.1:n.590+61C>A
NM_006579.2:c.469+61C>A NP_006570.1:n.469+61C>A
NM_006579.3:c.469+61C>A MANE Select NP_006570.1:n.469+61C>A
Search 100 bp 5'
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