Canonical Allele Identifier: CA315897048
Gene: PREX1 HGNC NCBI

Linked Data

dbSNP Id: rs1009279647
MyVariant Identifiers: chr20:g.47379674C>T (hg19) chr20:g.48763137C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.48763137C>T , CM000682.2:g.48763137C>T GRCh38
NC_000020.10:g.47379674C>T , CM000682.1:g.47379674C>T GRCh37
NC_000020.9:g.46813081C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371941.4:c.220-15257G>A MANE Select ENSP00000361009.3:n.220-15257G>A
ENST00000371941.3:c.220-15257G>A ENSP00000361009.3:n.220-15257G>A
NM_020820.3:c.220-15257G>A NP_065871.2:n.220-15257G>A
NM_020820.4:c.220-15257G>A MANE Select NP_065871.3:n.220-15257G>A
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