Canonical Allele Identifier: CA1588626996
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1753411659

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145353915A>C , CM000667.2:g.145353915A>C GRCh38
NC_000005.9:g.144733478A>C , CM000667.1:g.144733478A>C GRCh37
NC_000005.8:g.144713671A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944308.1:n.795-15538T>G