Canonical Allele Identifier: CA1588775059

Gene: PRELID2

Linked Data

• dbSNP Id: rs1754446852

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145659168T>G , CM000667.2:g.145659168T>G	GRCh38
NC_000005.9:g.145038731T>G , CM000667.1:g.145038731T>G	GRCh37
NC_000005.8:g.145018924T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.70+105763A>C
XR_944308.1:n.662+105763A>C
XM_017009130.1:c.*6188A>C	XP_016864619.1:n.*6188A>C
XM_017009133.1:c.*6220A>C	XP_016864622.1:n.*6220A>C
XR_001742025.1:n.913+44807A>C