Canonical Allele Identifier: CA412852952
Gene: EBP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.48386684G>C (hg19) chrX:g.48528296G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528296G>C , CM000685.2:g.48528296G>C GRCh38
NC_000023.10:g.48386684G>C , CM000685.1:g.48386684G>C GRCh37
NC_000023.9:g.48271628G>C NCBI36
NG_007452.1:g.11521G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.532G>C MANE Select ENSP00000417052.1:p.Glu178Gln
ENST00000651615.1:c.469+1011G>C ENSP00000498524.1:n.469+1011G>C
ENST00000276096.10:n.490G>C
ENST00000495186.5:c.532G>C ENSP00000417052.1:p.Glu178Gln
ENST00000498425.1:n.653G>C
NM_006579.2:c.532G>C NP_006570.1:p.Glu178Gln
NM_006579.3:c.532G>C MANE Select NP_006570.1:p.Glu178Gln
Search 100 bp 5'
Search 100 bp 3'