Canonical Allele Identifier: CA412850662

Gene: EBP

Linked Data

• MyVariant Identifiers: chrX:g.48382164C>G (hg19) ; chrX:g.48523776C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48523776C>G , CM000685.2:g.48523776C>G	GRCh38
NC_000023.10:g.48382164C>G , CM000685.1:g.48382164C>G	GRCh37
NC_000023.9:g.48267108C>G	NCBI36
NG_007452.1:g.7001C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000495186.6:c.5C>G MANE Select	ENSP00000417052.1:p.Thr2Ser
ENST00000651615.1:c.5C>G	ENSP00000498524.1:p.Thr2Ser
ENST00000276096.10:n.110-147C>G
ENST00000414061.1:c.5C>G	ENSP00000405832.1:p.Thr2Ser
ENST00000446158.5:c.5C>G	ENSP00000390031.1:p.Thr2Ser
ENST00000495186.5:c.5C>G	ENSP00000417052.1:p.Thr2Ser
ENST00000498425.1:n.126C>G
NM_006579.2:c.5C>G	NP_006570.1:p.Thr2Ser
NM_006579.3:c.5C>G MANE Select	NP_006570.1:p.Thr2Ser