Canonical Allele Identifier: CA129497613

Gene: PRELID2

Linked Data

• dbSNP Id: rs912281255
• gnomAD v3: 5-145353938-A-G
• gnomAD v4: 5-145353938-A-G
• MyVariant Identifiers: chr5:g.144733501A>G (hg19) ; chr5:g.145353938A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145353938A>G , CM000667.2:g.145353938A>G	GRCh38
NC_000005.9:g.144733501A>G , CM000667.1:g.144733501A>G	GRCh37
NC_000005.8:g.144713694A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944308.1:n.795-15561T>C