Canonical Allele Identifier: CA2686252165
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992603-G-GC
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992603_16992604insC , CM000670.2:g.16992603_16992604insC GRCh38
NC_000008.10:g.16850112_16850113insC , CM000670.1:g.16850112_16850113insC GRCh37
NC_000008.9:g.16894483_16894484insC NCBI36
NG_015978.1:g.14562_14563insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*468_*469insG MANE Select ENSP00000180166.5:n.*468_*469insG
ENST00000180166.5:c.*468_*469insG ENSP00000180166.5:n.*468_*469insG
NM_019851.3:c.*468_*469insG MANE Select NP_062825.1:n.*468_*469insG
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