Canonical Allele Identifier: CA1767396255
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993222G= , CM000670.2:g.16993222G= GRCh38
NC_000008.10:g.16850731G= , CM000670.1:g.16850731G= GRCh37
NC_000008.9:g.16895102G= NCBI36
NG_015978.1:g.13944C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.486C= MANE Select ENSP00000180166.5:p.Gly162=
ENST00000180166.5:c.486C= ENSP00000180166.5:p.Gly162=
ENST00000519941.1:c.190C=
NM_019851.2:c.486C= NP_062825.1:p.Gly162=
NM_019851.3:c.486C= MANE Select NP_062825.1:p.Gly162=