Canonical Allele Identifier: CA129525395

Gene: PRELID2

Linked Data

• dbSNP Id: rs115380590
• gnomAD v2: 5-144965312-T-C
• gnomAD v3: 5-145585749-T-C
• gnomAD v4: 5-145585749-T-C
• MyVariant Identifiers: chr5:g.144965312T>C (hg19) ; chr5:g.145585749T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145585749T>C , CM000667.2:g.145585749T>C	GRCh38
NC_000005.9:g.144965312T>C , CM000667.1:g.144965312T>C	GRCh37
NC_000005.8:g.144945505T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510259.5:n.71-112434A>G
XR_944308.1:n.662+179182A>G