Canonical Allele Identifier: CA129525448
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs148722622
gnomAD v2: 5-144965670-G-C
gnomAD v3: 5-145586107-G-C
gnomAD v4: 5-145586107-G-C
MyVariant Identifiers: chr5:g.144965670G>C (hg19) chr5:g.145586107G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586107G>C , CM000667.2:g.145586107G>C GRCh38
NC_000005.9:g.144965670G>C , CM000667.1:g.144965670G>C GRCh37
NC_000005.8:g.144945863G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112792C>G
XR_944308.1:n.662+178824C>G
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