Canonical Allele Identifier: CA2367752742
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs1215510900

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763190C>T , CM000682.2:g.48763190C>T GRCh38
NC_000020.10:g.47379727C>T , CM000682.1:g.47379727C>T GRCh37
NC_000020.9:g.46813134C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15310G>A MANE Select ENSP00000361009.3:n.220-15310G>A
ENST00000371941.3:c.220-15310G>A ENSP00000361009.3:n.220-15310G>A
NM_020820.3:c.220-15310G>A NP_065871.2:n.220-15310G>A
NM_020820.4:c.220-15310G>A MANE Select NP_065871.3:n.220-15310G>A