Canonical Allele Identifier: CA516016908
Gene: EBP HGNC NCBI

Linked Data

dbSNP Id: rs1311773570
MyVariant Identifiers: chrX:g.48386683A>G (hg19) chrX:g.48528295A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528295A>G , CM000685.2:g.48528295A>G GRCh38
NC_000023.10:g.48386683A>G , CM000685.1:g.48386683A>G GRCh37
NC_000023.9:g.48271627A>G NCBI36
NG_007452.1:g.11520A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.531A>G MANE Select ENSP00000417052.1:p.Gly177=
ENST00000651615.1:c.469+1010A>G ENSP00000498524.1:n.469+1010A>G
ENST00000276096.10:n.489A>G
ENST00000495186.5:c.531A>G ENSP00000417052.1:p.Gly177=
ENST00000498425.1:n.652A>G
NM_006579.2:c.531A>G NP_006570.1:p.Gly177=
NM_006579.3:c.531A>G MANE Select NP_006570.1:p.Gly177=
Search 100 bp 5'
Search 100 bp 3'