Canonical Allele Identifier: CA1588740132
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1753152375
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586118A>T , CM000667.2:g.145586118A>T GRCh38
NC_000005.9:g.144965681A>T , CM000667.1:g.144965681A>T GRCh37
NC_000005.8:g.144945874A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112803T>A
XR_944308.1:n.662+178813T>A
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