Canonical Allele Identifier: CA412852922
Gene: EBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528289G>T , CM000685.2:g.48528289G>T GRCh38
NC_000023.10:g.48386677G>T , CM000685.1:g.48386677G>T GRCh37
NC_000023.9:g.48271621G>T NCBI36
NG_007452.1:g.11514G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.525G>T MANE Select ENSP00000417052.1:p.Gln175His
ENST00000651615.1:c.469+1004G>T ENSP00000498524.1:n.469+1004G>T
ENST00000276096.10:n.483G>T
ENST00000495186.5:c.525G>T ENSP00000417052.1:p.Gln175His
ENST00000498425.1:n.646G>T
NM_006579.2:c.525G>T NP_006570.1:p.Gln175His
NM_006579.3:c.525G>T MANE Select NP_006570.1:p.Gln175His