Canonical Allele Identifier: CA1588775087
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659240T= , CM000667.2:g.145659240T= GRCh38
NC_000005.9:g.145038803T= , CM000667.1:g.145038803T= GRCh37
NC_000005.8:g.145018996T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105691A=
XR_944308.1:n.662+105691A=
XM_017009130.1:c.*6116A= XP_016864619.1:n.*6116A=
XM_017009133.1:c.*6148A= XP_016864622.1:n.*6148A=
XR_001742025.1:n.913+44735A=