Canonical Allele Identifier: CA1767395421
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992530T= , CM000670.2:g.16992530T= GRCh38
NC_000008.10:g.16850039T= , CM000670.1:g.16850039T= GRCh37
NC_000008.9:g.16894410T= NCBI36
NG_015978.1:g.14636A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*542A= MANE Select ENSP00000180166.5:n.*542A=
ENST00000180166.5:c.*542A= ENSP00000180166.5:n.*542A=
NM_019851.3:c.*542A= MANE Select NP_062825.1:n.*542A=
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