Canonical Allele Identifier: CA1767396147
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993143G= , CM000670.2:g.16993143G= GRCh38
NC_000008.10:g.16850652G= , CM000670.1:g.16850652G= GRCh37
NC_000008.9:g.16895023G= NCBI36
NG_015978.1:g.14023C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.565C= MANE Select ENSP00000180166.5:p.His189=
ENST00000180166.5:c.565C= ENSP00000180166.5:p.His189=
ENST00000519941.1:c.269C=
NM_019851.2:c.565C= NP_062825.1:p.His189=
NM_019851.3:c.565C= MANE Select NP_062825.1:p.His189=