Canonical Allele Identifier: CA805163871

Gene: PRELID2

Linked Data

• dbSNP Id: rs1187848805
• gnomAD v3: 5-145585939-A-G
• gnomAD v4: 5-145585939-A-G
• MyVariant Identifiers: chr5:g.144965502A>G (hg19) ; chr5:g.145585939A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145585939A>G , CM000667.2:g.145585939A>G	GRCh38
NC_000005.9:g.144965502A>G , CM000667.1:g.144965502A>G	GRCh37
NC_000005.8:g.144945695A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510259.5:n.71-112624T>C
XR_944308.1:n.662+178992T>C