Canonical Allele Identifier: CA75934191
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs948853984
gnomAD v2: 3-59691687-T-A
gnomAD v3: 3-59705961-T-A
gnomAD v4: 3-59705961-T-A
MyVariant Identifiers: chr3:g.59691687T>A (hg19) chr3:g.59705961T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705961T>A , CM000665.2:g.59705961T>A GRCh38
NC_000003.11:g.59691687T>A , CM000665.1:g.59691687T>A GRCh37
NC_000003.10:g.59666727T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103771T>A
Search 100 bp 5'
Search 100 bp 3'