Canonical Allele Identifier: CA1767396249
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993220C= , CM000670.2:g.16993220C= GRCh38
NC_000008.10:g.16850729C= , CM000670.1:g.16850729C= GRCh37
NC_000008.9:g.16895100C= NCBI36
NG_015978.1:g.13946G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.488G= MANE Select ENSP00000180166.5:p.Arg163=
ENST00000180166.5:c.488G= ENSP00000180166.5:p.Arg163=
ENST00000519941.1:c.192G=
NM_019851.2:c.488G= NP_062825.1:p.Arg163=
NM_019851.3:c.488G= MANE Select NP_062825.1:p.Arg163=