Canonical Allele Identifier: CA1767395505
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992608T= , CM000670.2:g.16992608T= GRCh38
NC_000008.10:g.16850117T= , CM000670.1:g.16850117T= GRCh37
NC_000008.9:g.16894488T= NCBI36
NG_015978.1:g.14558A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*464A= MANE Select ENSP00000180166.5:n.*464A=
ENST00000180166.5:c.*464A= ENSP00000180166.5:n.*464A=
NM_019851.3:c.*464A= MANE Select NP_062825.1:n.*464A=