Canonical Allele Identifier: CA908843238
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1365635819
gnomAD v3: 3-59705523-A-T
gnomAD v4: 3-59705523-A-T
MyVariant Identifiers: chr3:g.59691249A>T (hg19) chr3:g.59705523A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705523A>T , CM000665.2:g.59705523A>T GRCh38
NC_000003.11:g.59691249A>T , CM000665.1:g.59691249A>T GRCh37
NC_000003.10:g.59666289A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-104209A>T
Search 100 bp 5'
Search 100 bp 3'