Canonical Allele Identifier: CA2428298577
Gene: EBP HGNC NCBI

Linked Data

dbSNP Id: rs2061784576
gnomAD v4: X-48528149-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528149A>T , CM000685.2:g.48528149A>T GRCh38
NC_000023.10:g.48386537A>T , CM000685.1:g.48386537A>T GRCh37
NC_000023.9:g.48271481A>T NCBI36
NG_007452.1:g.11374A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.470-85A>T MANE Select ENSP00000417052.1:n.470-85A>T
ENST00000651615.1:c.469+864A>T ENSP00000498524.1:n.469+864A>T
ENST00000276096.10:n.428-85A>T
ENST00000446158.5:c.470-85A>T ENSP00000390031.1:n.470-85A>T
ENST00000495186.5:c.470-85A>T ENSP00000417052.1:n.470-85A>T
ENST00000498425.1:n.591-85A>T
NM_006579.2:c.470-85A>T NP_006570.1:n.470-85A>T
NM_006579.3:c.470-85A>T MANE Select NP_006570.1:n.470-85A>T