Canonical Allele Identifier: CA636097947
Gene: PREX1 HGNC NCBI

Linked Data

gnomAD v2: 20-47379747-T-C
gnomAD v3: 20-48763210-T-C
gnomAD v4: 20-48763210-T-C
MyVariant Identifiers: chr20:g.47379747T>C (hg19) chr20:g.48763210T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763210T>C , CM000682.2:g.48763210T>C GRCh38
NC_000020.10:g.47379747T>C , CM000682.1:g.47379747T>C GRCh37
NC_000020.9:g.46813154T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15330A>G MANE Select ENSP00000361009.3:n.220-15330A>G
ENST00000371941.3:c.220-15330A>G ENSP00000361009.3:n.220-15330A>G
NM_020820.3:c.220-15330A>G NP_065871.2:n.220-15330A>G
NM_020820.4:c.220-15330A>G MANE Select NP_065871.3:n.220-15330A>G
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