Canonical Allele Identifier: CA805163876
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1210688931
MyVariant Identifiers: chr5:g.144965533C>G (hg19) chr5:g.145585970C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585970C>G , CM000667.2:g.145585970C>G GRCh38
NC_000005.9:g.144965533C>G , CM000667.1:g.144965533C>G GRCh37
NC_000005.8:g.144945726C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112655G>C
XR_944308.1:n.662+178961G>C
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