Canonical Allele Identifier: CA805163850

Gene: PRELID2

Linked Data

• dbSNP Id: rs1312079719
• gnomAD v3: 5-145585882-G-A
• gnomAD v4: 5-145585882-G-A
• MyVariant Identifiers: chr5:g.144965445G>A (hg19) ; chr5:g.145585882G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145585882G>A , CM000667.2:g.145585882G>A	GRCh38
NC_000005.9:g.144965445G>A , CM000667.1:g.144965445G>A	GRCh37
NC_000005.8:g.144945638G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510259.5:n.71-112567C>T
XR_944308.1:n.662+179049C>T