Canonical Allele Identifier: CA1082551457
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1029586439

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585890C>G , CM000667.2:g.145585890C>G GRCh38
NC_000005.9:g.144965453C>G , CM000667.1:g.144965453C>G GRCh37
NC_000005.8:g.144945646C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112575G>C
XR_944308.1:n.662+179041G>C