Canonical Allele Identifier: CA2710338930

Gene: PRELID2

Linked Data

• dbSNP Id: rs2149675946

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145659217C>G , CM000667.2:g.145659217C>G	GRCh38
NC_000005.9:g.145038780C>G , CM000667.1:g.145038780C>G	GRCh37
NC_000005.8:g.145018973C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.70+105714G>C
XR_944308.1:n.662+105714G>C
XM_017009130.1:c.*6139G>C	XP_016864619.1:n.*6139G>C
XM_017009133.1:c.*6171G>C	XP_016864622.1:n.*6171G>C
XR_001742025.1:n.913+44758G>C