Canonical Allele Identifier: CA2367752749
Gene: PREX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763208G= , CM000682.2:g.48763208G= GRCh38
NC_000020.10:g.47379745G= , CM000682.1:g.47379745G= GRCh37
NC_000020.9:g.46813152G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15328C= MANE Select ENSP00000361009.3:n.220-15328C=
ENST00000371941.3:c.220-15328C= ENSP00000361009.3:n.220-15328C=
NM_020820.3:c.220-15328C= NP_065871.2:n.220-15328C=
NM_020820.4:c.220-15328C= MANE Select NP_065871.3:n.220-15328C=