Canonical Allele Identifier: CA805163955
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1325843028
gnomAD v3: 5-145586166-G-A
gnomAD v4: 5-145586166-G-A
MyVariant Identifiers: chr5:g.144965729G>A (hg19) chr5:g.145586166G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586166G>A , CM000667.2:g.145586166G>A GRCh38
NC_000005.9:g.144965729G>A , CM000667.1:g.144965729G>A GRCh37
NC_000005.8:g.144945922G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112851C>T
XR_944308.1:n.662+178765C>T
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