Canonical Allele Identifier: CA1018160510
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs2090192540
gnomAD v3: 20-48763342-T-A
gnomAD v4: 20-48763342-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763342T>A , CM000682.2:g.48763342T>A GRCh38
NC_000020.10:g.47379879T>A , CM000682.1:g.47379879T>A GRCh37
NC_000020.9:g.46813286T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15462A>T MANE Select ENSP00000361009.3:n.220-15462A>T
ENST00000371941.3:c.220-15462A>T ENSP00000361009.3:n.220-15462A>T
NM_020820.3:c.220-15462A>T NP_065871.2:n.220-15462A>T
NM_020820.4:c.220-15462A>T MANE Select NP_065871.3:n.220-15462A>T
Search 100 bp 5'
Search 100 bp 3'