Canonical Allele Identifier: CA1767395362
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992451C= , CM000670.2:g.16992451C= GRCh38
NC_000008.10:g.16849960C= , CM000670.1:g.16849960C= GRCh37
NC_000008.9:g.16894331C= NCBI36
NG_015978.1:g.14715G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*621G= MANE Select ENSP00000180166.5:n.*621G=
ENST00000180166.5:c.*621G= ENSP00000180166.5:n.*621G=
NM_019851.3:c.*621G= MANE Select NP_062825.1:n.*621G=
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