Canonical Allele Identifier: CA745109673
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs1337381980
gnomAD v3: 20-48763345-G-C
gnomAD v4: 20-48763345-G-C
MyVariant Identifiers: chr20:g.47379882G>C (hg19) chr20:g.48763345G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763345G>C , CM000682.2:g.48763345G>C GRCh38
NC_000020.10:g.47379882G>C , CM000682.1:g.47379882G>C GRCh37
NC_000020.9:g.46813289G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15465C>G MANE Select ENSP00000361009.3:n.220-15465C>G
ENST00000371941.3:c.220-15465C>G ENSP00000361009.3:n.220-15465C>G
NM_020820.3:c.220-15465C>G NP_065871.2:n.220-15465C>G
NM_020820.4:c.220-15465C>G MANE Select NP_065871.3:n.220-15465C>G
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