Canonical Allele Identifier: CA129497608
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs26160
gnomAD v2: 5-144733456-T-C
gnomAD v3: 5-145353893-T-C
gnomAD v4: 5-145353893-T-C
MyVariant Identifiers: chr5:g.144733456T>C (hg19) chr5:g.145353893T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145353893T>C , CM000667.2:g.145353893T>C GRCh38
NC_000005.9:g.144733456T>C , CM000667.1:g.144733456T>C GRCh37
NC_000005.8:g.144713649T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944308.1:n.795-15516A>G
Search 100 bp 5'
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