Canonical Allele Identifier: CA1767395302
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992384A= , CM000670.2:g.16992384A= GRCh38
NC_000008.10:g.16849893A= , CM000670.1:g.16849893A= GRCh37
NC_000008.9:g.16894264A= NCBI36
NG_015978.1:g.14782T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*688T= MANE Select ENSP00000180166.5:n.*688T=
ENST00000180166.5:c.*688T= ENSP00000180166.5:n.*688T=
NM_019851.3:c.*688T= MANE Select NP_062825.1:n.*688T=
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