Canonical Allele Identifier: CA563215406
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1207440360
gnomAD v2: 5-144965350-T-A
gnomAD v3: 5-145585787-T-A
gnomAD v4: 5-145585787-T-A
MyVariant Identifiers: chr5:g.144965350T>A (hg19) chr5:g.145585787T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585787T>A , CM000667.2:g.145585787T>A GRCh38
NC_000005.9:g.144965350T>A , CM000667.1:g.144965350T>A GRCh37
NC_000005.8:g.144945543T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112472A>T
XR_944308.1:n.662+179144A>T
Search 100 bp 5'
Search 100 bp 3'