Canonical Allele Identifier: CA1767395422
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992531C= , CM000670.2:g.16992531C= GRCh38
NC_000008.10:g.16850040C= , CM000670.1:g.16850040C= GRCh37
NC_000008.9:g.16894411C= NCBI36
NG_015978.1:g.14635G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*541G= MANE Select ENSP00000180166.5:n.*541G=
ENST00000180166.5:c.*541G= ENSP00000180166.5:n.*541G=
NM_019851.3:c.*541G= MANE Select NP_062825.1:n.*541G=