Canonical Allele Identifier: CA2816588196
Gene: PREX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763228G>T , CM000682.2:g.48763228G>T GRCh38
NC_000020.10:g.47379765G>T , CM000682.1:g.47379765G>T GRCh37
NC_000020.9:g.46813172G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371941.4:c.220-15348C>A MANE Select ENSP00000361009.3:n.220-15348C>A
ENST00000371941.3:c.220-15348C>A ENSP00000361009.3:n.220-15348C>A
NM_020820.3:c.220-15348C>A NP_065871.2:n.220-15348C>A
NM_020820.4:c.220-15348C>A MANE Select NP_065871.3:n.220-15348C>A