Canonical Allele Identifier: CA1767395497
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992604T= , CM000670.2:g.16992604T= GRCh38
NC_000008.10:g.16850113T= , CM000670.1:g.16850113T= GRCh37
NC_000008.9:g.16894484T= NCBI36
NG_015978.1:g.14562A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*468A= MANE Select ENSP00000180166.5:n.*468A=
ENST00000180166.5:c.*468A= ENSP00000180166.5:n.*468A=
NM_019851.3:c.*468A= MANE Select NP_062825.1:n.*468A=