Canonical Allele Identifier: CA1767395433
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992543A= , CM000670.2:g.16992543A= GRCh38
NC_000008.10:g.16850052A= , CM000670.1:g.16850052A= GRCh37
NC_000008.9:g.16894423A= NCBI36
NG_015978.1:g.14623T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*529T= MANE Select ENSP00000180166.5:n.*529T=
ENST00000180166.5:c.*529T= ENSP00000180166.5:n.*529T=
NM_019851.3:c.*529T= MANE Select NP_062825.1:n.*529T=