Canonical Allele Identifier: CA129525402
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1042647382
gnomAD v3: 5-145585808-G-T
gnomAD v4: 5-145585808-G-T
MyVariant Identifiers: chr5:g.144965371G>T (hg19) chr5:g.145585808G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585808G>T , CM000667.2:g.145585808G>T GRCh38
NC_000005.9:g.144965371G>T , CM000667.1:g.144965371G>T GRCh37
NC_000005.8:g.144945564G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.71-112493C>A
XR_944308.1:n.662+179123C>A
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