Canonical Allele Identifier: CA129525398
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs904787290
gnomAD v2: 5-144965326-C-T
gnomAD v3: 5-145585763-C-T
gnomAD v4: 5-145585763-C-T
MyVariant Identifiers: chr5:g.144965326C>T (hg19) chr5:g.145585763C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585763C>T , CM000667.2:g.145585763C>T GRCh38
NC_000005.9:g.144965326C>T , CM000667.1:g.144965326C>T GRCh37
NC_000005.8:g.144945519C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112448G>A
XR_944308.1:n.662+179168G>A
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