Canonical Allele Identifier: CA1588775069
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659198A= , CM000667.2:g.145659198A= GRCh38
NC_000005.9:g.145038761A= , CM000667.1:g.145038761A= GRCh37
NC_000005.8:g.145018954A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105733T=
XR_944308.1:n.662+105733T=
XM_017009130.1:c.*6158T= XP_016864619.1:n.*6158T=
XM_017009133.1:c.*6190T= XP_016864622.1:n.*6190T=
XR_001742025.1:n.913+44777T=