Canonical Allele Identifier: CA1767396124
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993129T= , CM000670.2:g.16993129T= GRCh38
NC_000008.10:g.16850638T= , CM000670.1:g.16850638T= GRCh37
NC_000008.9:g.16895009T= NCBI36
NG_015978.1:g.14037A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.579A= MANE Select ENSP00000180166.5:p.Arg193=
ENST00000180166.5:c.579A= ENSP00000180166.5:p.Arg193=
ENST00000519941.1:c.283A=
NM_019851.2:c.579A= NP_062825.1:p.Arg193=
NM_019851.3:c.579A= MANE Select NP_062825.1:p.Arg193=