Canonical Allele Identifier: CA805163856
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1397966902
MyVariant Identifiers: chr5:g.144965461T>C (hg19) chr5:g.145585898T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585898T>C , CM000667.2:g.145585898T>C GRCh38
NC_000005.9:g.144965461T>C , CM000667.1:g.144965461T>C GRCh37
NC_000005.8:g.144945654T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112583A>G
XR_944308.1:n.662+179033A>G
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