Canonical Allele Identifier: CA543450407
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1404624129
gnomAD v2: 3-59691766-A-G
gnomAD v3: 3-59706040-A-G
gnomAD v4: 3-59706040-A-G
MyVariant Identifiers: chr3:g.59691766A>G (hg19) chr3:g.59706040A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706040A>G , CM000665.2:g.59706040A>G GRCh38
NC_000003.11:g.59691766A>G , CM000665.1:g.59691766A>G GRCh37
NC_000003.10:g.59666806A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103692A>G
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