Canonical Allele Identifier: CA2367752713
Gene: PREX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763134T= , CM000682.2:g.48763134T= GRCh38
NC_000020.10:g.47379671T= , CM000682.1:g.47379671T= GRCh37
NC_000020.9:g.46813078T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371941.4:c.220-15254A= MANE Select ENSP00000361009.3:n.220-15254A=
ENST00000371941.3:c.220-15254A= ENSP00000361009.3:n.220-15254A=
NM_020820.3:c.220-15254A= NP_065871.2:n.220-15254A=
NM_020820.4:c.220-15254A= MANE Select NP_065871.3:n.220-15254A=