Canonical Allele Identifier: CA1767395501
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992605T= , CM000670.2:g.16992605T= GRCh38
NC_000008.10:g.16850114T= , CM000670.1:g.16850114T= GRCh37
NC_000008.9:g.16894485T= NCBI36
NG_015978.1:g.14561A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*467A= MANE Select ENSP00000180166.5:n.*467A=
ENST00000180166.5:c.*467A= ENSP00000180166.5:n.*467A=
NM_019851.3:c.*467A= MANE Select NP_062825.1:n.*467A=