Canonical Allele Identifier: CA1767396131
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993131T= , CM000670.2:g.16993131T= GRCh38
NC_000008.10:g.16850640T= , CM000670.1:g.16850640T= GRCh37
NC_000008.9:g.16895011T= NCBI36
NG_015978.1:g.14035A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.577A= MANE Select ENSP00000180166.5:p.Arg193=
ENST00000180166.5:c.577A= ENSP00000180166.5:p.Arg193=
ENST00000519941.1:c.281A=
NM_019851.2:c.577A= NP_062825.1:p.Arg193=
NM_019851.3:c.577A= MANE Select NP_062825.1:p.Arg193=