Canonical Allele Identifier: CA129525452
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs748574763
gnomAD v3: 5-145586131-A-C
gnomAD v4: 5-145586131-A-C
MyVariant Identifiers: chr5:g.144965694A>C (hg19) chr5:g.145586131A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586131A>C , CM000667.2:g.145586131A>C GRCh38
NC_000005.9:g.144965694A>C , CM000667.1:g.144965694A>C GRCh37
NC_000005.8:g.144945887A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112816T>G
XR_944308.1:n.662+178800T>G
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