Canonical Allele Identifier: CA129525441

Gene: PRELID2

Linked Data

• dbSNP Id: rs548657409
• gnomAD v2: 5-144965600-C-A
• gnomAD v3: 5-145586037-C-A
• gnomAD v4: 5-145586037-C-A
• MyVariant Identifiers: chr5:g.144965600C>A (hg19) ; chr5:g.145586037C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145586037C>A , CM000667.2:g.145586037C>A	GRCh38
NC_000005.9:g.144965600C>A , CM000667.1:g.144965600C>A	GRCh37
NC_000005.8:g.144945793C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510259.5:n.71-112722G>T
XR_944308.1:n.662+178894G>T