Canonical Allele Identifier: CA129525396
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1028498613
MyVariant Identifiers: chr5:g.144965315C>T (hg19) chr5:g.145585752C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585752C>T , CM000667.2:g.145585752C>T GRCh38
NC_000005.9:g.144965315C>T , CM000667.1:g.144965315C>T GRCh37
NC_000005.8:g.144945508C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.71-112437G>A
XR_944308.1:n.662+179179G>A
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