Canonical Allele Identifier: CA1588775064

Gene: PRELID2

Linked Data

• dbSNP Id: rs1754447013

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145659182G>A , CM000667.2:g.145659182G>A	GRCh38
NC_000005.9:g.145038745G>A , CM000667.1:g.145038745G>A	GRCh37
NC_000005.8:g.145018938G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.70+105749C>T
XR_944308.1:n.662+105749C>T
XM_017009130.1:c.*6174C>T	XP_016864619.1:n.*6174C>T
XM_017009133.1:c.*6206C>T	XP_016864622.1:n.*6206C>T
XR_001742025.1:n.913+44793C>T