Canonical Allele Identifier: CA1588775079

Gene: PRELID2

Linked Data

• dbSNP Id: rs1754447753

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145659227A>G , CM000667.2:g.145659227A>G	GRCh38
NC_000005.9:g.145038790A>G , CM000667.1:g.145038790A>G	GRCh37
NC_000005.8:g.145018983A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.70+105704T>C
XR_944308.1:n.662+105704T>C
XM_017009130.1:c.*6129T>C	XP_016864619.1:n.*6129T>C
XM_017009133.1:c.*6161T>C	XP_016864622.1:n.*6161T>C
XR_001742025.1:n.913+44748T>C