Canonical Allele Identifier: CA908843578
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1300871602
gnomAD v3: 3-59706094-C-T
gnomAD v4: 3-59706094-C-T
MyVariant Identifiers: chr3:g.59691820C>T (hg19) chr3:g.59706094C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706094C>T , CM000665.2:g.59706094C>T GRCh38
NC_000003.11:g.59691820C>T , CM000665.1:g.59691820C>T GRCh37
NC_000003.10:g.59666860C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103638C>T
Search 100 bp 5'
Search 100 bp 3'