Canonical Allele Identifier: CA2820807633

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527466A>T , CM000685.2:g.48527466A>T	GRCh38
NC_000023.10:g.48385854A>T , CM000685.1:g.48385854A>T	GRCh37
NC_000023.9:g.48270798A>T	NCBI36
NG_007452.1:g.10691A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.469+181A>T MANE Select	ENSP00000417052.1:n.469+181A>T
ENST00000651615.1:c.469+181A>T	ENSP00000498524.1:n.469+181A>T
ENST00000276096.10:n.427+181A>T
ENST00000446158.5:c.469+181A>T	ENSP00000390031.1:n.469+181A>T
ENST00000466461.1:n.489A>T
ENST00000495186.5:c.469+181A>T	ENSP00000417052.1:n.469+181A>T
ENST00000498425.1:n.590+181A>T
NM_006579.2:c.469+181A>T	NP_006570.1:n.469+181A>T
NM_006579.3:c.469+181A>T MANE Select	NP_006570.1:n.469+181A>T