Canonical Allele Identifier: CA2549942809
Gene: PREX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763091T>C , CM000682.2:g.48763091T>C GRCh38
NC_000020.10:g.47379628T>C , CM000682.1:g.47379628T>C GRCh37
NC_000020.9:g.46813035T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371941.4:c.220-15211A>G MANE Select ENSP00000361009.3:n.220-15211A>G
ENST00000371941.3:c.220-15211A>G ENSP00000361009.3:n.220-15211A>G
NM_020820.3:c.220-15211A>G NP_065871.2:n.220-15211A>G
NM_020820.4:c.220-15211A>G MANE Select NP_065871.3:n.220-15211A>G