Canonical Allele Identifier: CA1767395641
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992777C= , CM000670.2:g.16992777C= GRCh38
NC_000008.10:g.16850286C= , CM000670.1:g.16850286C= GRCh37
NC_000008.9:g.16894657C= NCBI36
NG_015978.1:g.14389G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*295G= MANE Select ENSP00000180166.5:n.*295G=
ENST00000180166.5:c.*295G= ENSP00000180166.5:n.*295G=
NM_019851.3:c.*295G= MANE Select NP_062825.1:n.*295G=
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