Canonical Allele Identifier: CA745109632
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs1270941065
gnomAD v3: 20-48763234-A-T
gnomAD v4: 20-48763234-A-T
MyVariant Identifiers: chr20:g.47379771A>T (hg19) chr20:g.48763234A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763234A>T , CM000682.2:g.48763234A>T GRCh38
NC_000020.10:g.47379771A>T , CM000682.1:g.47379771A>T GRCh37
NC_000020.9:g.46813178A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15354T>A MANE Select ENSP00000361009.3:n.220-15354T>A
ENST00000371941.3:c.220-15354T>A ENSP00000361009.3:n.220-15354T>A
NM_020820.3:c.220-15354T>A NP_065871.2:n.220-15354T>A
NM_020820.4:c.220-15354T>A MANE Select NP_065871.3:n.220-15354T>A
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