Canonical Allele Identifier: CA75934172
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1044597288
gnomAD v3: 3-59705794-T-C
gnomAD v4: 3-59705794-T-C
MyVariant Identifiers: chr3:g.59691520T>C (hg19) chr3:g.59705794T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705794T>C , CM000665.2:g.59705794T>C GRCh38
NC_000003.11:g.59691520T>C , CM000665.1:g.59691520T>C GRCh37
NC_000003.10:g.59666560T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103938T>C
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