Canonical Allele Identifier: CA1588775062

Gene: PRELID2

Linked Data

• dbSNP Id: rs1754446954

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145659179C>A , CM000667.2:g.145659179C>A	GRCh38
NC_000005.9:g.145038742C>A , CM000667.1:g.145038742C>A	GRCh37
NC_000005.8:g.145018935C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.70+105752G>T
XR_944308.1:n.662+105752G>T
XM_017009130.1:c.*6177G>T	XP_016864619.1:n.*6177G>T
XM_017009133.1:c.*6209G>T	XP_016864622.1:n.*6209G>T
XR_001742025.1:n.913+44796G>T