Canonical Allele Identifier: CA1767396266
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993227T= , CM000670.2:g.16993227T= GRCh38
NC_000008.10:g.16850736T= , CM000670.1:g.16850736T= GRCh37
NC_000008.9:g.16895107T= NCBI36
NG_015978.1:g.13939A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.481A= MANE Select ENSP00000180166.5:p.Thr161=
ENST00000180166.5:c.481A= ENSP00000180166.5:p.Thr161=
ENST00000519941.1:c.185A=
NM_019851.2:c.481A= NP_062825.1:p.Thr161=
NM_019851.3:c.481A= MANE Select NP_062825.1:p.Thr161=