Canonical Allele Identifier: CA1588775081

Gene: PRELID2

Linked Data

• dbSNP Id: rs1754447808

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145659228T>C , CM000667.2:g.145659228T>C	GRCh38
NC_000005.9:g.145038791T>C , CM000667.1:g.145038791T>C	GRCh37
NC_000005.8:g.145018984T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.70+105703A>G
XR_944308.1:n.662+105703A>G
XM_017009130.1:c.*6128A>G	XP_016864619.1:n.*6128A>G
XM_017009133.1:c.*6160A>G	XP_016864622.1:n.*6160A>G
XR_001742025.1:n.913+44747A>G