Canonical Allele Identifier: CA805163902
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1292905391
gnomAD v3: 5-145586026-G-T
gnomAD v4: 5-145586026-G-T
MyVariant Identifiers: chr5:g.144965589G>T (hg19) chr5:g.145586026G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586026G>T , CM000667.2:g.145586026G>T GRCh38
NC_000005.9:g.144965589G>T , CM000667.1:g.144965589G>T GRCh37
NC_000005.8:g.144945782G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112711C>A
XR_944308.1:n.662+178905C>A
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