Canonical Allele Identifier: CA1767395506
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992614T= , CM000670.2:g.16992614T= GRCh38
NC_000008.10:g.16850123T= , CM000670.1:g.16850123T= GRCh37
NC_000008.9:g.16894494T= NCBI36
NG_015978.1:g.14552A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*458A= MANE Select ENSP00000180166.5:n.*458A=
ENST00000180166.5:c.*458A= ENSP00000180166.5:n.*458A=
NM_019851.3:c.*458A= MANE Select NP_062825.1:n.*458A=