Canonical Allele Identifier: CA875916549
Gene: EBP HGNC NCBI

Linked Data

dbSNP Id: rs1173152756
gnomAD v3: X-48528127-A-G
gnomAD v4: X-48528127-A-G
MyVariant Identifiers: chrX:g.48528127A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528127A>G , CM000685.2:g.48528127A>G GRCh38
NC_000023.10:g.48386515A>G , CM000685.1:g.48386515A>G GRCh37
NC_000023.9:g.48271459A>G NCBI36
NG_007452.1:g.11352A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.470-107A>G MANE Select ENSP00000417052.1:n.470-107A>G
ENST00000651615.1:c.469+842A>G ENSP00000498524.1:n.469+842A>G
ENST00000276096.10:n.428-107A>G
ENST00000446158.5:c.470-107A>G ENSP00000390031.1:n.470-107A>G
ENST00000495186.5:c.470-107A>G ENSP00000417052.1:n.470-107A>G
ENST00000498425.1:n.591-107A>G
NM_006579.2:c.470-107A>G NP_006570.1:n.470-107A>G
NM_006579.3:c.470-107A>G MANE Select NP_006570.1:n.470-107A>G