Canonical Allele Identifier: CA1588740126
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1024768850
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586101T>G , CM000667.2:g.145586101T>G GRCh38
NC_000005.9:g.144965664T>G , CM000667.1:g.144965664T>G GRCh37
NC_000005.8:g.144945857T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112786A>C
XR_944308.1:n.662+178830A>C
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