Canonical Allele Identifier: CA2367752702
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs776583205

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763115T>G , CM000682.2:g.48763115T>G GRCh38
NC_000020.10:g.47379652T>G , CM000682.1:g.47379652T>G GRCh37
NC_000020.9:g.46813059T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371941.4:c.220-15235A>C MANE Select ENSP00000361009.3:n.220-15235A>C
ENST00000371941.3:c.220-15235A>C ENSP00000361009.3:n.220-15235A>C
NM_020820.3:c.220-15235A>C NP_065871.2:n.220-15235A>C
NM_020820.4:c.220-15235A>C MANE Select NP_065871.3:n.220-15235A>C