Allele Registry

Canonical Allele Identifier: CA12065896

Gene: PRELID2 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr5:g.145544941T>C

GRCh37 chr5:g.144924504T>C

Linked Data - Sequence & Population

gnomAD v2:

5:144924504 T / C

gnomAD v3:

5:145544941 T / C

gnomAD v4:

chr5-145544941-T-C

Joint Max Group AF 0.17715139 (NFE)

Genomes Max Group AF 0.17715139 (NFE)

Linked Data - NCBI & NCI

dbSNP:

7713855

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145544941T>C , CM000667.2:g.145544941T>C	GRCh38
NC_000005.9:g.144924504T>C , CM000667.1:g.144924504T>C	GRCh37
NC_000005.8:g.144904697T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510259.5:n.71-71626A>G
XR_944308.1:n.663-163223A>G

Search 100 bp 5'

Search 100 bp 3'