Canonical Allele Identifier: CA1767396246
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993219_16993220delinsGC , CM000670.2:g.16993219_16993220delinsGC GRCh38
NC_000008.10:g.16850728_16850729delinsGC , CM000670.1:g.16850728_16850729delinsGC GRCh37
NC_000008.9:g.16895099_16895100delinsGC NCBI36
NG_015978.1:g.13946_13947delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.488_489delinsGC MANE Select ENSP00000180166.5:p.Arg163=
ENST00000180166.5:c.488_489delinsGC ENSP00000180166.5:p.Arg163=
ENST00000519941.1:c.192_193delinsGC
NM_019851.2:c.488_489delinsGC NP_062825.1:p.Arg163=
NM_019851.3:c.488_489delinsGC MANE Select NP_062825.1:p.Arg163=
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