Canonical Allele Identifier: CA1767395337
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992427_16992428delinsGT , CM000670.2:g.16992427_16992428delinsGT GRCh38
NC_000008.10:g.16849936_16849937delinsGT , CM000670.1:g.16849936_16849937delinsGT GRCh37
NC_000008.9:g.16894307_16894308delinsGT NCBI36
NG_015978.1:g.14738_14739delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*644_*645delinsAC MANE Select ENSP00000180166.5:n.*644_*645delinsAC
ENST00000180166.5:c.*644_*645delinsAC ENSP00000180166.5:n.*644_*645delinsAC
NM_019851.3:c.*644_*645delinsAC MANE Select NP_062825.1:n.*644_*645delinsAC
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