Canonical Allele Identifier: CA412850888
Gene: EBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48523827A>C , CM000685.2:g.48523827A>C GRCh38
NC_000023.10:g.48382215A>C , CM000685.1:g.48382215A>C GRCh37
NC_000023.9:g.48267159A>C NCBI36
NG_007452.1:g.7052A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.56A>C MANE Select ENSP00000417052.1:p.Asp19Ala
ENST00000651615.1:c.56A>C ENSP00000498524.1:p.Asp19Ala
ENST00000276096.10:n.110-96A>C
ENST00000414061.1:c.56A>C ENSP00000405832.1:p.Asp19Ala
ENST00000446158.5:c.56A>C ENSP00000390031.1:p.Asp19Ala
ENST00000495186.5:c.56A>C ENSP00000417052.1:p.Asp19Ala
ENST00000498425.1:n.177A>C
NM_006579.2:c.56A>C NP_006570.1:p.Asp19Ala
NM_006579.3:c.56A>C MANE Select NP_006570.1:p.Asp19Ala