Canonical Allele Identifier: CA2693633139
Gene: EBP HGNC NCBI

Linked Data

gnomAD v4: X-48528137-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528137C>T , CM000685.2:g.48528137C>T GRCh38
NC_000023.10:g.48386525C>T , CM000685.1:g.48386525C>T GRCh37
NC_000023.9:g.48271469C>T NCBI36
NG_007452.1:g.11362C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.470-97C>T MANE Select ENSP00000417052.1:n.470-97C>T
ENST00000651615.1:c.469+852C>T ENSP00000498524.1:n.469+852C>T
ENST00000276096.10:n.428-97C>T
ENST00000446158.5:c.470-97C>T ENSP00000390031.1:n.470-97C>T
ENST00000495186.5:c.470-97C>T ENSP00000417052.1:n.470-97C>T
ENST00000498425.1:n.591-97C>T
NM_006579.2:c.470-97C>T NP_006570.1:n.470-97C>T
NM_006579.3:c.470-97C>T MANE Select NP_006570.1:n.470-97C>T