Canonical Allele Identifier: CA75934173
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs767906247
gnomAD v2: 3-59691522-G-T
gnomAD v3: 3-59705796-G-T
gnomAD v4: 3-59705796-G-T
MyVariant Identifiers: chr3:g.59691522G>T (hg19) chr3:g.59705796G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705796G>T , CM000665.2:g.59705796G>T GRCh38
NC_000003.11:g.59691522G>T , CM000665.1:g.59691522G>T GRCh37
NC_000003.10:g.59666562G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103936G>T
Search 100 bp 5'
Search 100 bp 3'