Canonical Allele Identifier: CA1767396157
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993153C= , CM000670.2:g.16993153C= GRCh38
NC_000008.10:g.16850662C= , CM000670.1:g.16850662C= GRCh37
NC_000008.9:g.16895033C= NCBI36
NG_015978.1:g.14013G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.555G= MANE Select ENSP00000180166.5:p.Gln185=
ENST00000180166.5:c.555G= ENSP00000180166.5:p.Gln185=
ENST00000519941.1:c.259G=
NM_019851.2:c.555G= NP_062825.1:p.Gln185=
NM_019851.3:c.555G= MANE Select NP_062825.1:p.Gln185=