Canonical Allele Identifier: CA1588739939
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs543805965

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585697C>G , CM000667.2:g.145585697C>G GRCh38
NC_000005.9:g.144965260C>G , CM000667.1:g.144965260C>G GRCh37
NC_000005.8:g.144945453C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112382G>C
XR_944308.1:n.662+179234G>C