Canonical Allele Identifier: CA1082548879
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1754447420

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659198A>G , CM000667.2:g.145659198A>G GRCh38
NC_000005.9:g.145038761A>G , CM000667.1:g.145038761A>G GRCh37
NC_000005.8:g.145018954A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105733T>C
XR_944308.1:n.662+105733T>C
XM_017009130.1:c.*6158T>C XP_016864619.1:n.*6158T>C
XM_017009133.1:c.*6190T>C XP_016864622.1:n.*6190T>C
XR_001742025.1:n.913+44777T>C