Canonical Allele Identifier: CA129525400
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1000296859
gnomAD v3: 5-145585772-T-C
gnomAD v4: 5-145585772-T-C
MyVariant Identifiers: chr5:g.144965335T>C (hg19) chr5:g.145585772T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585772T>C , CM000667.2:g.145585772T>C GRCh38
NC_000005.9:g.144965335T>C , CM000667.1:g.144965335T>C GRCh37
NC_000005.8:g.144945528T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.71-112457A>G
XR_944308.1:n.662+179159A>G
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