Canonical Allele Identifier: CA2693633170
Gene: EBP HGNC NCBI

Linked Data

gnomAD v4: X-48528184-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528184A>G , CM000685.2:g.48528184A>G GRCh38
NC_000023.10:g.48386572A>G , CM000685.1:g.48386572A>G GRCh37
NC_000023.9:g.48271516A>G NCBI36
NG_007452.1:g.11409A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.470-50A>G MANE Select ENSP00000417052.1:n.470-50A>G
ENST00000651615.1:c.469+899A>G ENSP00000498524.1:n.469+899A>G
ENST00000276096.10:n.428-50A>G
ENST00000446158.5:c.470-50A>G ENSP00000390031.1:n.470-50A>G
ENST00000495186.5:c.470-50A>G ENSP00000417052.1:n.470-50A>G
ENST00000498425.1:n.591-50A>G
NM_006579.2:c.470-50A>G NP_006570.1:n.470-50A>G
NM_006579.3:c.470-50A>G MANE Select NP_006570.1:n.470-50A>G