Canonical Allele Identifier: CA412850653
Gene: EBP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.48382162G>A (hg19) chrX:g.48523774G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48523774G>A , CM000685.2:g.48523774G>A GRCh38
NC_000023.10:g.48382162G>A , CM000685.1:g.48382162G>A GRCh37
NC_000023.9:g.48267106G>A NCBI36
NG_007452.1:g.6999G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.3G>A MANE Select ENSP00000417052.1:p.Met1Ile
ENST00000651615.1:c.3G>A ENSP00000498524.1:p.Met1Ile
ENST00000276096.10:n.110-149G>A
ENST00000414061.1:c.3G>A ENSP00000405832.1:p.Met1Ile
ENST00000446158.5:c.3G>A ENSP00000390031.1:p.Met1Ile
ENST00000495186.5:c.3G>A ENSP00000417052.1:p.Met1Ile
ENST00000498425.1:n.124G>A
NM_006579.2:c.3G>A NP_006570.1:p.Met1Ile
NM_006579.3:c.3G>A MANE Select NP_006570.1:p.Met1Ile
Search 100 bp 5'
Search 100 bp 3'