Canonical Allele Identifier: CA1588775085
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659236G= , CM000667.2:g.145659236G= GRCh38
NC_000005.9:g.145038799G= , CM000667.1:g.145038799G= GRCh37
NC_000005.8:g.145018992G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105695C=
XR_944308.1:n.662+105695C=
XM_017009130.1:c.*6120C= XP_016864619.1:n.*6120C=
XM_017009133.1:c.*6152C= XP_016864622.1:n.*6152C=
XR_001742025.1:n.913+44739C=