Canonical Allele Identifier: CA563215428
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs116421900
gnomAD v2: 5-144965710-G-T
gnomAD v3: 5-145586147-G-T
gnomAD v4: 5-145586147-G-T
MyVariant Identifiers: chr5:g.144965710G>T (hg19) chr5:g.145586147G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586147G>T , CM000667.2:g.145586147G>T GRCh38
NC_000005.9:g.144965710G>T , CM000667.1:g.144965710G>T GRCh37
NC_000005.8:g.144945903G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112832C>A
XR_944308.1:n.662+178784C>A
Search 100 bp 5'
Search 100 bp 3'