Canonical Allele Identifier: CA563215403
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1358669678
gnomAD v2: 5-144965323-C-A
gnomAD v3: 5-145585760-C-A
gnomAD v4: 5-145585760-C-A
MyVariant Identifiers: chr5:g.144965323C>A (hg19) chr5:g.145585760C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585760C>A , CM000667.2:g.145585760C>A GRCh38
NC_000005.9:g.144965323C>A , CM000667.1:g.144965323C>A GRCh37
NC_000005.8:g.144945516C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112445G>T
XR_944308.1:n.662+179171G>T
Search 100 bp 5'
Search 100 bp 3'