Canonical Allele Identifier: CA129525422
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs915188606
gnomAD v2: 5-144965553-CT-C
gnomAD v3: 5-145585990-CT-C
gnomAD v4: 5-145585990-CT-C
MyVariant Identifiers: chr5:g.144965554del (hg19) chr5:g.145585991del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585991del , CM000667.2:g.145585991del GRCh38
NC_000005.9:g.144965554del , CM000667.1:g.144965554del GRCh37
NC_000005.8:g.144945747del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112676del
XR_944308.1:n.662+178940del
Search 100 bp 5'
Search 100 bp 3'