Canonical Allele Identifier: CA1018160516
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs989089208

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763344G>C , CM000682.2:g.48763344G>C GRCh38
NC_000020.10:g.47379881G>C , CM000682.1:g.47379881G>C GRCh37
NC_000020.9:g.46813288G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371941.4:c.220-15464C>G MANE Select ENSP00000361009.3:n.220-15464C>G
ENST00000371941.3:c.220-15464C>G ENSP00000361009.3:n.220-15464C>G
NM_020820.3:c.220-15464C>G NP_065871.2:n.220-15464C>G
NM_020820.4:c.220-15464C>G MANE Select NP_065871.3:n.220-15464C>G