Canonical Allele Identifier: CA1767396224
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993195T= , CM000670.2:g.16993195T= GRCh38
NC_000008.10:g.16850704T= , CM000670.1:g.16850704T= GRCh37
NC_000008.9:g.16895075T= NCBI36
NG_015978.1:g.13971A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.513A= MANE Select ENSP00000180166.5:p.Lys171=
ENST00000180166.5:c.513A= ENSP00000180166.5:p.Lys171=
ENST00000519941.1:c.217A=
NM_019851.2:c.513A= NP_062825.1:p.Lys171=
NM_019851.3:c.513A= MANE Select NP_062825.1:p.Lys171=