Canonical Allele Identifier: CA1048502789
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700186994
gnomAD v3: 3-59706061-T-C
gnomAD v4: 3-59706061-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706061T>C , CM000665.2:g.59706061T>C GRCh38
NC_000003.11:g.59691787T>C , CM000665.1:g.59691787T>C GRCh37
NC_000003.10:g.59666827T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103671T>C