Canonical Allele Identifier: CA412851457

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48523955C>T , CM000685.2:g.48523955C>T	GRCh38
NC_000023.10:g.48382343C>T , CM000685.1:g.48382343C>T	GRCh37
NC_000023.9:g.48267287C>T	NCBI36
NG_007452.1:g.7180C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006579.3:c.184C>T MANE Select	NP_006570.1:p.Arg62Trp
ENST00000495186.6:c.184C>T MANE Select	ENSP00000417052.1:p.Arg62Trp
NM_006579.2:c.184C>T	NP_006570.1:p.Arg62Trp
ENST00000276096.10:n.142C>T
ENST00000414061.1:c.184C>T	ENSP00000405832.1:p.Arg62Trp
ENST00000446158.5:c.184C>T	ENSP00000390031.1:p.Arg62Trp
ENST00000495186.5:c.184C>T	ENSP00000417052.1:p.Arg62Trp
ENST00000498425.1:n.305C>T
ENST00000651615.1:c.184C>T	ENSP00000498524.1:p.Arg62Trp