Canonical Allele Identifier: CA1588775078
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659227A= , CM000667.2:g.145659227A= GRCh38
NC_000005.9:g.145038790A= , CM000667.1:g.145038790A= GRCh37
NC_000005.8:g.145018983A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105704T=
XR_944308.1:n.662+105704T=
XM_017009130.1:c.*6129T= XP_016864619.1:n.*6129T=
XM_017009133.1:c.*6161T= XP_016864622.1:n.*6161T=
XR_001742025.1:n.913+44748T=