Canonical Allele Identifier: CA1767395435
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992544A= , CM000670.2:g.16992544A= GRCh38
NC_000008.10:g.16850053A= , CM000670.1:g.16850053A= GRCh37
NC_000008.9:g.16894424A= NCBI36
NG_015978.1:g.14622T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*528T= MANE Select ENSP00000180166.5:n.*528T=
ENST00000180166.5:c.*528T= ENSP00000180166.5:n.*528T=
NM_019851.3:c.*528T= MANE Select NP_062825.1:n.*528T=