Canonical Allele Identifier: CA1767395788
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992904_16992905delinsCA , CM000670.2:g.16992904_16992905delinsCA GRCh38
NC_000008.10:g.16850413_16850414delinsCA , CM000670.1:g.16850413_16850414delinsCA GRCh37
NC_000008.9:g.16894784_16894785delinsCA NCBI36
NG_015978.1:g.14261_14262delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*167_*168delinsTG MANE Select ENSP00000180166.5:n.*167_*168delinsTG
ENST00000180166.5:c.*167_*168delinsTG ENSP00000180166.5:n.*167_*168delinsTG
NM_019851.2:c.*167_*168delinsTG NP_062825.1:n.*167_*168delinsTG
NM_019851.3:c.*167_*168delinsTG MANE Select NP_062825.1:n.*167_*168delinsTG
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