Canonical Allele Identifier: CA1588775065

Gene: PRELID2

Linked Data

• dbSNP Id: rs1754447065

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145659185A>T , CM000667.2:g.145659185A>T	GRCh38
NC_000005.9:g.145038748A>T , CM000667.1:g.145038748A>T	GRCh37
NC_000005.8:g.145018941A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.70+105746T>A
XR_944308.1:n.662+105746T>A
XM_017009130.1:c.*6171T>A	XP_016864619.1:n.*6171T>A
XM_017009133.1:c.*6203T>A	XP_016864622.1:n.*6203T>A
XR_001742025.1:n.913+44790T>A