Canonical Allele Identifier: CA1588775075

Gene: PRELID2

Linked Data

• dbSNP Id: rs1754447633

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145659211C>T , CM000667.2:g.145659211C>T	GRCh38
NC_000005.9:g.145038774C>T , CM000667.1:g.145038774C>T	GRCh37
NC_000005.8:g.145018967C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.70+105720G>A
XR_944308.1:n.662+105720G>A
XM_017009130.1:c.*6145G>A	XP_016864619.1:n.*6145G>A
XM_017009133.1:c.*6177G>A	XP_016864622.1:n.*6177G>A
XR_001742025.1:n.913+44764G>A