Canonical Allele Identifier: CA805163839

Gene: PRELID2

Linked Data

• dbSNP Id: rs1200617923
• gnomAD v3: 5-145585841-G-A
• gnomAD v4: 5-145585841-G-A
• MyVariant Identifiers: chr5:g.144965404G>A (hg19) ; chr5:g.145585841G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145585841G>A , CM000667.2:g.145585841G>A	GRCh38
NC_000005.9:g.144965404G>A , CM000667.1:g.144965404G>A	GRCh37
NC_000005.8:g.144945597G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.71-112526C>T
XR_944308.1:n.662+179090C>T