Canonical Allele Identifier: CA1767396141
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993138G= , CM000670.2:g.16993138G= GRCh38
NC_000008.10:g.16850647G= , CM000670.1:g.16850647G= GRCh37
NC_000008.9:g.16895018G= NCBI36
NG_015978.1:g.14028C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.570C= MANE Select ENSP00000180166.5:p.Phe190=
ENST00000180166.5:c.570C= ENSP00000180166.5:p.Phe190=
ENST00000519941.1:c.274C=
NM_019851.2:c.570C= NP_062825.1:p.Phe190=
NM_019851.3:c.570C= MANE Select NP_062825.1:p.Phe190=