Canonical Allele Identifier: CA563227629
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1391407411

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659241G>A , CM000667.2:g.145659241G>A GRCh38
NC_000005.9:g.145038804G>A , CM000667.1:g.145038804G>A GRCh37
NC_000005.8:g.145018997G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105690C>T
XR_944308.1:n.662+105690C>T
XM_017009130.1:c.*6115C>T XP_016864619.1:n.*6115C>T
XM_017009133.1:c.*6147C>T XP_016864622.1:n.*6147C>T
XR_001742025.1:n.913+44734C>T