Canonical Allele Identifier: CA129525436
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs534832574

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586032A>C , CM000667.2:g.145586032A>C GRCh38
NC_000005.9:g.144965595A>C , CM000667.1:g.144965595A>C GRCh37
NC_000005.8:g.144945788A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112717T>G
XR_944308.1:n.662+178899T>G