Canonical Allele Identifier: CA805163896

Gene: PRELID2

Linked Data

• dbSNP Id: rs1190871599
• MyVariant Identifiers: chr5:g.144965585C>T (hg19) ; chr5:g.145586022C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145586022C>T , CM000667.2:g.145586022C>T	GRCh38
NC_000005.9:g.144965585C>T , CM000667.1:g.144965585C>T	GRCh37
NC_000005.8:g.144945778C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510259.5:n.71-112707G>A
XR_944308.1:n.662+178909G>A