Canonical Allele Identifier: CA2367752766
Gene: PREX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763248A= , CM000682.2:g.48763248A= GRCh38
NC_000020.10:g.47379785A= , CM000682.1:g.47379785A= GRCh37
NC_000020.9:g.46813192A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371941.4:c.220-15368T= MANE Select ENSP00000361009.3:n.220-15368T=
ENST00000371941.3:c.220-15368T= ENSP00000361009.3:n.220-15368T=
NM_020820.3:c.220-15368T= NP_065871.2:n.220-15368T=
NM_020820.4:c.220-15368T= MANE Select NP_065871.3:n.220-15368T=