Canonical Allele Identifier: CA543450136
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1450185429
gnomAD v2: 3-59691428-G-A
gnomAD v3: 3-59705702-G-A
gnomAD v4: 3-59705702-G-A
MyVariant Identifiers: chr3:g.59691428G>A (hg19) chr3:g.59705702G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705702G>A , CM000665.2:g.59705702G>A GRCh38
NC_000003.11:g.59691428G>A , CM000665.1:g.59691428G>A GRCh37
NC_000003.10:g.59666468G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-104030G>A
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