Canonical Allele Identifier: CA1767395581
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992713G= , CM000670.2:g.16992713G= GRCh38
NC_000008.10:g.16850222G= , CM000670.1:g.16850222G= GRCh37
NC_000008.9:g.16894593G= NCBI36
NG_015978.1:g.14453C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*359C= MANE Select ENSP00000180166.5:n.*359C=
ENST00000180166.5:c.*359C= ENSP00000180166.5:n.*359C=
NM_019851.3:c.*359C= MANE Select NP_062825.1:n.*359C=