Canonical Allele Identifier: CA2736909257

Gene: PREX1

Linked Data

• dbSNP Id: rs2122849264

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.48763353C>T , CM000682.2:g.48763353C>T	GRCh38
NC_000020.10:g.47379890C>T , CM000682.1:g.47379890C>T	GRCh37
NC_000020.9:g.46813297C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371941.4:c.220-15473G>A MANE Select	ENSP00000361009.3:n.220-15473G>A
ENST00000371941.3:c.220-15473G>A	ENSP00000361009.3:n.220-15473G>A
NM_020820.3:c.220-15473G>A	NP_065871.2:n.220-15473G>A
NM_020820.4:c.220-15473G>A MANE Select	NP_065871.3:n.220-15473G>A