Canonical Allele Identifier: CA129525438

Gene: PRELID2

Linked Data

• dbSNP Id: rs200435080
• MyVariant Identifiers: chr5:g.144965596A>C (hg19) ; chr5:g.145586033A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145586033A>C , CM000667.2:g.145586033A>C	GRCh38
NC_000005.9:g.144965596A>C , CM000667.1:g.144965596A>C	GRCh37
NC_000005.8:g.144945789A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510259.5:n.71-112718T>G
XR_944308.1:n.662+178898T>G