Canonical Allele Identifier: CA1767395411
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992519G= , CM000670.2:g.16992519G= GRCh38
NC_000008.10:g.16850028G= , CM000670.1:g.16850028G= GRCh37
NC_000008.9:g.16894399G= NCBI36
NG_015978.1:g.14647C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*553C= MANE Select ENSP00000180166.5:n.*553C=
ENST00000180166.5:c.*553C= ENSP00000180166.5:n.*553C=
NM_019851.3:c.*553C= MANE Select NP_062825.1:n.*553C=
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