Canonical Allele Identifier: CA10403043
Gene: EBP HGNC NCBI

Linked Data

dbSNP Id: rs782419794
gnomAD v2: X-48386571-A-G
gnomAD v3: X-48528183-A-G
gnomAD v4: X-48528183-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528183A>G , CM000685.2:g.48528183A>G GRCh38
NC_000023.10:g.48386571A>G , CM000685.1:g.48386571A>G GRCh37
NC_000023.9:g.48271515A>G NCBI36
NG_007452.1:g.11408A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.470-51A>G MANE Select ENSP00000417052.1:n.470-51A>G
ENST00000651615.1:c.469+898A>G ENSP00000498524.1:n.469+898A>G
ENST00000276096.10:n.428-51A>G
ENST00000446158.5:c.470-51A>G ENSP00000390031.1:n.470-51A>G
ENST00000495186.5:c.470-51A>G ENSP00000417052.1:n.470-51A>G
ENST00000498425.1:n.591-51A>G
NM_006579.2:c.470-51A>G NP_006570.1:n.470-51A>G
NM_006579.3:c.470-51A>G MANE Select NP_006570.1:n.470-51A>G