Canonical Allele Identifier: CA1767396264
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993226G= , CM000670.2:g.16993226G= GRCh38
NC_000008.10:g.16850735G= , CM000670.1:g.16850735G= GRCh37
NC_000008.9:g.16895106G= NCBI36
NG_015978.1:g.13940C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.482C= MANE Select ENSP00000180166.5:p.Thr161=
ENST00000180166.5:c.482C= ENSP00000180166.5:p.Thr161=
ENST00000519941.1:c.186C=
NM_019851.2:c.482C= NP_062825.1:p.Thr161=
NM_019851.3:c.482C= MANE Select NP_062825.1:p.Thr161=