Canonical Allele Identifier: CA516014781

Gene: EBP

Linked Data

• MyVariant Identifiers: chrX:g.48385387T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48526999T>C , CM000685.2:g.48526999T>C	GRCh38
NC_000023.10:g.48385387T>C , CM000685.1:g.48385387T>C	GRCh37
NC_000023.9:g.48270331T>C	NCBI36
NG_007452.1:g.10224T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.312T>C MANE Select	ENSP00000417052.1:p.Tyr104=
ENST00000651615.1:c.312T>C	ENSP00000498524.1:p.Tyr104=
ENST00000276096.10:n.270T>C
ENST00000414061.1:c.312T>C	ENSP00000405832.1:p.Tyr104=
ENST00000446158.5:c.312T>C	ENSP00000390031.1:p.Tyr104=
ENST00000466461.1:n.151T>C
ENST00000495186.5:c.312T>C	ENSP00000417052.1:p.Tyr104=
ENST00000498425.1:n.433T>C
NM_006579.2:c.312T>C	NP_006570.1:p.Tyr104=
NM_006579.3:c.312T>C MANE Select	NP_006570.1:p.Tyr104=