Canonical Allele Identifier: CA1767395331
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992420T= , CM000670.2:g.16992420T= GRCh38
NC_000008.10:g.16849929T= , CM000670.1:g.16849929T= GRCh37
NC_000008.9:g.16894300T= NCBI36
NG_015978.1:g.14746A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*652A= MANE Select ENSP00000180166.5:n.*652A=
ENST00000180166.5:c.*652A= ENSP00000180166.5:n.*652A=
NM_019851.3:c.*652A= MANE Select NP_062825.1:n.*652A=