Canonical Allele Identifier: CA2710340128
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs2149627691

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585784T>C , CM000667.2:g.145585784T>C GRCh38
NC_000005.9:g.144965347T>C , CM000667.1:g.144965347T>C GRCh37
NC_000005.8:g.144945540T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112469A>G
XR_944308.1:n.662+179147A>G