Canonical Allele Identifier: CA1588775072
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1581034080

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659203C>A , CM000667.2:g.145659203C>A GRCh38
NC_000005.9:g.145038766C>A , CM000667.1:g.145038766C>A GRCh37
NC_000005.8:g.145018959C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105728G>T
XR_944308.1:n.662+105728G>T
XM_017009130.1:c.*6153G>T XP_016864619.1:n.*6153G>T
XM_017009133.1:c.*6185G>T XP_016864622.1:n.*6185G>T
XR_001742025.1:n.913+44772G>T