Canonical Allele Identifier: CA1767396188
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993167A= , CM000670.2:g.16993167A= GRCh38
NC_000008.10:g.16850676A= , CM000670.1:g.16850676A= GRCh37
NC_000008.9:g.16895047A= NCBI36
NG_015978.1:g.13999T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.541T= MANE Select ENSP00000180166.5:p.Ser181=
ENST00000180166.5:c.541T= ENSP00000180166.5:p.Ser181=
ENST00000519941.1:c.245T=
NM_019851.2:c.541T= NP_062825.1:p.Ser181=
NM_019851.3:c.541T= MANE Select NP_062825.1:p.Ser181=