Canonical Allele Identifier: CA563215427
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1320341519
gnomAD v2: 5-144965683-T-G
gnomAD v3: 5-145586120-T-G
gnomAD v4: 5-145586120-T-G
MyVariant Identifiers: chr5:g.144965683T>G (hg19) chr5:g.145586120T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586120T>G , CM000667.2:g.145586120T>G GRCh38
NC_000005.9:g.144965683T>G , CM000667.1:g.144965683T>G GRCh37
NC_000005.8:g.144945876T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112805A>C
XR_944308.1:n.662+178811A>C
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