Canonical Allele Identifier: CA315897166
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs2426087

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763274G>A , CM000682.2:g.48763274G>A GRCh38
NC_000020.10:g.47379811G>A , CM000682.1:g.47379811G>A GRCh37
NC_000020.9:g.46813218G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15394C>T MANE Select ENSP00000361009.3:n.220-15394C>T
ENST00000371941.3:c.220-15394C>T ENSP00000361009.3:n.220-15394C>T
NM_020820.3:c.220-15394C>T NP_065871.2:n.220-15394C>T
NM_020820.4:c.220-15394C>T MANE Select NP_065871.3:n.220-15394C>T