Canonical Allele Identifier: CA1767395308
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992387C= , CM000670.2:g.16992387C= GRCh38
NC_000008.10:g.16849896C= , CM000670.1:g.16849896C= GRCh37
NC_000008.9:g.16894267C= NCBI36
NG_015978.1:g.14779G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*685G= MANE Select ENSP00000180166.5:n.*685G=
ENST00000180166.5:c.*685G= ENSP00000180166.5:n.*685G=
NM_019851.3:c.*685G= MANE Select NP_062825.1:n.*685G=
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