Canonical Allele Identifier: CA412852676

Gene: EBP

Linked Data

• ClinVar Variation Id: 988320
• ClinVar RCV Id: RCV001269598
• dbSNP Id: rs2061782205
• MyVariant Identifiers: chrX:g.48385673G>A (hg19) ; chrX:g.48527285G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527285G>A , CM000685.2:g.48527285G>A	GRCh38
NC_000023.10:g.48385673G>A , CM000685.1:g.48385673G>A	GRCh37
NC_000023.9:g.48270617G>A	NCBI36
NG_007452.1:g.10510G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.469G>A MANE Select	ENSP00000417052.1:p.Gly157Ser
ENST00000651615.1:c.469G>A	ENSP00000498524.1:p.Glu157Lys
ENST00000276096.10:n.427G>A
ENST00000446158.5:c.469G>A	ENSP00000390031.1:p.Gly157Ser
ENST00000466461.1:n.308G>A
ENST00000495186.5:c.469G>A	ENSP00000417052.1:p.Gly157Ser
ENST00000498425.1:n.590G>A
NM_006579.2:c.469G>A	NP_006570.1:p.Gly157Ser
NM_006579.3:c.469G>A MANE Select	NP_006570.1:p.Gly157Ser