Canonical Allele Identifier: CA1048502800
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700187143
gnomAD v3: 3-59706091-T-G
gnomAD v4: 3-59706091-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706091T>G , CM000665.2:g.59706091T>G GRCh38
NC_000003.11:g.59691817T>G , CM000665.1:g.59691817T>G GRCh37
NC_000003.10:g.59666857T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103641T>G
Search 100 bp 5'
Search 100 bp 3'