Canonical Allele Identifier: CA745109649
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs1382445795
gnomAD v3: 20-48763265-C-G
gnomAD v4: 20-48763265-C-G
MyVariant Identifiers: chr20:g.47379802C>G (hg19) chr20:g.48763265C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763265C>G , CM000682.2:g.48763265C>G GRCh38
NC_000020.10:g.47379802C>G , CM000682.1:g.47379802C>G GRCh37
NC_000020.9:g.46813209C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371941.4:c.220-15385G>C MANE Select ENSP00000361009.3:n.220-15385G>C
ENST00000371941.3:c.220-15385G>C ENSP00000361009.3:n.220-15385G>C
NM_020820.3:c.220-15385G>C NP_065871.2:n.220-15385G>C
NM_020820.4:c.220-15385G>C MANE Select NP_065871.3:n.220-15385G>C
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