Canonical Allele Identifier: CA129525406
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs10074645

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585822C>T , CM000667.2:g.145585822C>T GRCh38
NC_000005.9:g.144965385C>T , CM000667.1:g.144965385C>T GRCh37
NC_000005.8:g.144945578C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.71-112507G>A
XR_944308.1:n.662+179109G>A