Canonical Allele Identifier: CA1588775107
Community Standard Title: NC_000005.10:g.145659268T=
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659268T= , CM000667.2:g.145659268T= GRCh38
NC_000005.9:g.145038831T= , CM000667.1:g.145038831T= GRCh37
NC_000005.8:g.145019024T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.70+105663A=
XM_017009130.1:c.*6088A= XP_016864619.1:n.*6088A=
XM_017009133.1:c.*6120A= XP_016864622.1:n.*6120A=
XR_001742025.1:n.913+44707A=
XR_944308.1:n.662+105663A=