Canonical Allele Identifier: CA129525439
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs531431294
MyVariant Identifiers: chr5:g.144965597del (hg19) chr5:g.145586034del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586034del , CM000667.2:g.145586034del GRCh38
NC_000005.9:g.144965597del , CM000667.1:g.144965597del GRCh37
NC_000005.8:g.144945790del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112719del
XR_944308.1:n.662+178897del
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