Canonical Allele Identifier: CA2693633147
Gene: EBP HGNC NCBI

Linked Data

gnomAD v4: X-48528151-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528151T>G , CM000685.2:g.48528151T>G GRCh38
NC_000023.10:g.48386539T>G , CM000685.1:g.48386539T>G GRCh37
NC_000023.9:g.48271483T>G NCBI36
NG_007452.1:g.11376T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.470-83T>G MANE Select ENSP00000417052.1:n.470-83T>G
ENST00000651615.1:c.469+866T>G ENSP00000498524.1:n.469+866T>G
ENST00000276096.10:n.428-83T>G
ENST00000446158.5:c.470-83T>G ENSP00000390031.1:n.470-83T>G
ENST00000495186.5:c.470-83T>G ENSP00000417052.1:n.470-83T>G
ENST00000498425.1:n.591-83T>G
NM_006579.2:c.470-83T>G NP_006570.1:n.470-83T>G
NM_006579.3:c.470-83T>G MANE Select NP_006570.1:n.470-83T>G