Canonical Allele Identifier: CA2428298348
Gene: EBP HGNC NCBI

Linked Data

dbSNP Id: rs2061782497

Genomic Alleles

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

Transcript Alleles

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