Canonical Allele Identifier: CA805163800
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1199949685
MyVariant Identifiers: chr5:g.144965339_144965350del (hg19) chr5:g.145585776_145585787del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585780_145585791del , CM000667.2:g.145585780_145585791del GRCh38
NC_000005.9:g.144965343_144965354del , CM000667.1:g.144965343_144965354del GRCh37
NC_000005.8:g.144945536_144945547del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112472_71-112461del
XR_944308.1:n.662+179144_662+179155del
Search 100 bp 5'
Search 100 bp 3'