Canonical Allele Identifier: CA315897131
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs73258434

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763236T>C , CM000682.2:g.48763236T>C GRCh38
NC_000020.10:g.47379773T>C , CM000682.1:g.47379773T>C GRCh37
NC_000020.9:g.46813180T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15356A>G MANE Select ENSP00000361009.3:n.220-15356A>G
ENST00000371941.3:c.220-15356A>G ENSP00000361009.3:n.220-15356A>G
NM_020820.3:c.220-15356A>G NP_065871.2:n.220-15356A>G
NM_020820.4:c.220-15356A>G MANE Select NP_065871.3:n.220-15356A>G