Canonical Allele Identifier: CA412852955
Gene: EBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528297A>C , CM000685.2:g.48528297A>C GRCh38
NC_000023.10:g.48386685A>C , CM000685.1:g.48386685A>C GRCh37
NC_000023.9:g.48271629A>C NCBI36
NG_007452.1:g.11522A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.533A>C MANE Select ENSP00000417052.1:p.Glu178Ala
ENST00000651615.1:c.469+1012A>C ENSP00000498524.1:n.469+1012A>C
ENST00000276096.10:n.491A>C
ENST00000495186.5:c.533A>C ENSP00000417052.1:p.Glu178Ala
ENST00000498425.1:n.654A>C
NM_006579.2:c.533A>C NP_006570.1:p.Glu178Ala
NM_006579.3:c.533A>C MANE Select NP_006570.1:p.Glu178Ala