Canonical Allele Identifier: CA908843562
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1191493752
MyVariant Identifiers: chr3:g.59691763A>T (hg19) chr3:g.59706037A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706037A>T , CM000665.2:g.59706037A>T GRCh38
NC_000003.11:g.59691763A>T , CM000665.1:g.59691763A>T GRCh37
NC_000003.10:g.59666803A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103695A>T
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Search 100 bp 3'