Canonical Allele Identifier: CA805163916
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs201010239

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586034T>C , CM000667.2:g.145586034T>C GRCh38
NC_000005.9:g.144965597T>C , CM000667.1:g.144965597T>C GRCh37
NC_000005.8:g.144945790T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112719A>G
XR_944308.1:n.662+178897A>G