Canonical Allele Identifier: CA129525447
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1024768850
gnomAD v2: 5-144965664-T-C
gnomAD v3: 5-145586101-T-C
gnomAD v4: 5-145586101-T-C
MyVariant Identifiers: chr5:g.144965664T>C (hg19) chr5:g.145586101T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586101T>C , CM000667.2:g.145586101T>C GRCh38
NC_000005.9:g.144965664T>C , CM000667.1:g.144965664T>C GRCh37
NC_000005.8:g.144945857T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112786A>G
XR_944308.1:n.662+178830A>G
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