Canonical Allele Identifier: CA412852357

Gene: EBP

Linked Data

• MyVariant Identifiers: chrX:g.48385569A>T (hg19) ; chrX:g.48527181A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527181A>T , CM000685.2:g.48527181A>T	GRCh38
NC_000023.10:g.48385569A>T , CM000685.1:g.48385569A>T	GRCh37
NC_000023.9:g.48270513A>T	NCBI36
NG_007452.1:g.10406A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.365A>T MANE Select	ENSP00000417052.1:p.Glu122Val
ENST00000651615.1:c.365A>T	ENSP00000498524.1:p.Glu122Val
ENST00000276096.10:n.323A>T
ENST00000414061.1:c.365A>T	ENSP00000405832.1:p.Glu122Val
ENST00000446158.5:c.365A>T	ENSP00000390031.1:p.Glu122Val
ENST00000466461.1:n.204A>T
ENST00000495186.5:c.365A>T	ENSP00000417052.1:p.Glu122Val
ENST00000498425.1:n.486A>T
NM_006579.2:c.365A>T	NP_006570.1:p.Glu122Val
NM_006579.3:c.365A>T MANE Select	NP_006570.1:p.Glu122Val