Canonical Allele Identifier: CA2367752758
Gene: PREX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763234A= , CM000682.2:g.48763234A= GRCh38
NC_000020.10:g.47379771A= , CM000682.1:g.47379771A= GRCh37
NC_000020.9:g.46813178A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15354T= MANE Select ENSP00000361009.3:n.220-15354T=
ENST00000371941.3:c.220-15354T= ENSP00000361009.3:n.220-15354T=
NM_020820.3:c.220-15354T= NP_065871.2:n.220-15354T=
NM_020820.4:c.220-15354T= MANE Select NP_065871.3:n.220-15354T=