Canonical Allele Identifier: CA563215402

Gene: PRELID2

Linked Data

• dbSNP Id: rs1447714530
• gnomAD v2: 5-144965298-A-G
• gnomAD v3: 5-145585735-A-G
• gnomAD v4: 5-145585735-A-G
• MyVariant Identifiers: chr5:g.144965298A>G (hg19) ; chr5:g.145585735A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145585735A>G , CM000667.2:g.145585735A>G	GRCh38
NC_000005.9:g.144965298A>G , CM000667.1:g.144965298A>G	GRCh37
NC_000005.8:g.144945491A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510259.5:n.71-112420T>C
XR_944308.1:n.662+179196T>C