Canonical Allele Identifier: CA129525411

Gene: PRELID2

Linked Data

• dbSNP Id: rs961087643
• MyVariant Identifiers: chr5:g.144965438A>C (hg19) ; chr5:g.145585875A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145585875A>C , CM000667.2:g.145585875A>C	GRCh38
NC_000005.9:g.144965438A>C , CM000667.1:g.144965438A>C	GRCh37
NC_000005.8:g.144945631A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510259.5:n.71-112560T>G
XR_944308.1:n.662+179056T>G