Canonical Allele Identifier: CA1767395473
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992586C= , CM000670.2:g.16992586C= GRCh38
NC_000008.10:g.16850095C= , CM000670.1:g.16850095C= GRCh37
NC_000008.9:g.16894466C= NCBI36
NG_015978.1:g.14580G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*486G= MANE Select ENSP00000180166.5:n.*486G=
ENST00000180166.5:c.*486G= ENSP00000180166.5:n.*486G=
NM_019851.3:c.*486G= MANE Select NP_062825.1:n.*486G=