Canonical Allele Identifier: CA129525431
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs201909904
MyVariant Identifiers: chr5:g.144965593_144965595del (hg19) chr5:g.145586030_145586032del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586030_145586032del , CM000667.2:g.145586030_145586032del GRCh38
NC_000005.9:g.144965593_144965595del , CM000667.1:g.144965593_144965595del GRCh37
NC_000005.8:g.144945786_144945788del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112717_71-112715del
XR_944308.1:n.662+178899_662+178901del
Search 100 bp 5'
Search 100 bp 3'