Canonical Allele Identifier: CA805163862
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1361167511
MyVariant Identifiers: chr5:g.144965475A>G (hg19) chr5:g.145585912A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585912A>G , CM000667.2:g.145585912A>G GRCh38
NC_000005.9:g.144965475A>G , CM000667.1:g.144965475A>G GRCh37
NC_000005.8:g.144945668A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112597T>C
XR_944308.1:n.662+179019T>C
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