Canonical Allele Identifier: CA412852662

Gene: EBP

Linked Data

• MyVariant Identifiers: chrX:g.48385665T>C (hg19) ; chrX:g.48527277T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527277T>C , CM000685.2:g.48527277T>C	GRCh38
NC_000023.10:g.48385665T>C , CM000685.1:g.48385665T>C	GRCh37
NC_000023.9:g.48270609T>C	NCBI36
NG_007452.1:g.10502T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.461T>C MANE Select	ENSP00000417052.1:p.Val154Ala
ENST00000651615.1:c.461T>C	ENSP00000498524.1:p.Val154Ala
ENST00000276096.10:n.419T>C
ENST00000446158.5:c.461T>C	ENSP00000390031.1:p.Val154Ala
ENST00000466461.1:n.300T>C
ENST00000495186.5:c.461T>C	ENSP00000417052.1:p.Val154Ala
ENST00000498425.1:n.582T>C
NM_006579.2:c.461T>C	NP_006570.1:p.Val154Ala
NM_006579.3:c.461T>C MANE Select	NP_006570.1:p.Val154Ala