Canonical Allele Identifier: CA1588775060
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659170A= , CM000667.2:g.145659170A= GRCh38
NC_000005.9:g.145038733A= , CM000667.1:g.145038733A= GRCh37
NC_000005.8:g.145018926A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105761T=
XR_944308.1:n.662+105761T=
XM_017009130.1:c.*6186T= XP_016864619.1:n.*6186T=
XM_017009133.1:c.*6218T= XP_016864622.1:n.*6218T=
XR_001742025.1:n.913+44805T=