Canonical Allele Identifier: CA1767396119
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993127G= , CM000670.2:g.16993127G= GRCh38
NC_000008.10:g.16850636G= , CM000670.1:g.16850636G= GRCh37
NC_000008.9:g.16895007G= NCBI36
NG_015978.1:g.14039C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.581C= MANE Select ENSP00000180166.5:p.Pro194=
ENST00000180166.5:c.581C= ENSP00000180166.5:p.Pro194=
ENST00000519941.1:c.285C=
NM_019851.2:c.581C= NP_062825.1:p.Pro194=
NM_019851.3:c.581C= MANE Select NP_062825.1:p.Pro194=