Canonical Allele Identifier: CA1767395297
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992379_16992380delinsGA , CM000670.2:g.16992379_16992380delinsGA GRCh38
NC_000008.10:g.16849888_16849889delinsGA , CM000670.1:g.16849888_16849889delinsGA GRCh37
NC_000008.9:g.16894259_16894260delinsGA NCBI36
NG_015978.1:g.14786_14787delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*692_*693delinsTC MANE Select ENSP00000180166.5:n.*692_*693delinsTC
ENST00000180166.5:c.*692_*693delinsTC ENSP00000180166.5:n.*692_*693delinsTC
NM_019851.3:c.*692_*693delinsTC MANE Select NP_062825.1:n.*692_*693delinsTC
Search 100 bp 5'
Search 100 bp 3'