Canonical Allele Identifier: CA1082551456
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs973020409

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585889C>T , CM000667.2:g.145585889C>T GRCh38
NC_000005.9:g.144965452C>T , CM000667.1:g.144965452C>T GRCh37
NC_000005.8:g.144945645C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112574G>A
XR_944308.1:n.662+179042G>A