Canonical Allele Identifier: CA1588740152
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1325843028

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586166G>C , CM000667.2:g.145586166G>C GRCh38
NC_000005.9:g.144965729G>C , CM000667.1:g.144965729G>C GRCh37
NC_000005.8:g.144945922G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112851C>G
XR_944308.1:n.662+178765C>G