Canonical Allele Identifier: CA745109607
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs1229463155

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763133A>C , CM000682.2:g.48763133A>C GRCh38
NC_000020.10:g.47379670A>C , CM000682.1:g.47379670A>C GRCh37
NC_000020.9:g.46813077A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371941.4:c.220-15253T>G MANE Select ENSP00000361009.3:n.220-15253T>G
ENST00000371941.3:c.220-15253T>G ENSP00000361009.3:n.220-15253T>G
NM_020820.3:c.220-15253T>G NP_065871.2:n.220-15253T>G
NM_020820.4:c.220-15253T>G MANE Select NP_065871.3:n.220-15253T>G