Canonical Allele Identifier: CA2367752695
Gene: PREX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763102T= , CM000682.2:g.48763102T= GRCh38
NC_000020.10:g.47379639T= , CM000682.1:g.47379639T= GRCh37
NC_000020.9:g.46813046T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15222A= MANE Select ENSP00000361009.3:n.220-15222A=
ENST00000371941.3:c.220-15222A= ENSP00000361009.3:n.220-15222A=
NM_020820.3:c.220-15222A= NP_065871.2:n.220-15222A=
NM_020820.4:c.220-15222A= MANE Select NP_065871.3:n.220-15222A=
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