Canonical Allele Identifier: CA1767396259
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993225A= , CM000670.2:g.16993225A= GRCh38
NC_000008.10:g.16850734A= , CM000670.1:g.16850734A= GRCh37
NC_000008.9:g.16895105A= NCBI36
NG_015978.1:g.13941T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.483T= MANE Select ENSP00000180166.5:p.Thr161=
ENST00000180166.5:c.483T= ENSP00000180166.5:p.Thr161=
ENST00000519941.1:c.187T=
NM_019851.2:c.483T= NP_062825.1:p.Thr161=
NM_019851.3:c.483T= MANE Select NP_062825.1:p.Thr161=