Canonical Allele Identifier: CA2367752696
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs2090190578
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Genomic Alleles

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

Transcript Alleles

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