Canonical Allele Identifier: CA1767396239
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993213A= , CM000670.2:g.16993213A= GRCh38
NC_000008.10:g.16850722A= , CM000670.1:g.16850722A= GRCh37
NC_000008.9:g.16895093A= NCBI36
NG_015978.1:g.13953T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.495T= MANE Select ENSP00000180166.5:p.Tyr165=
ENST00000180166.5:c.495T= ENSP00000180166.5:p.Tyr165=
ENST00000519941.1:c.199T=
NM_019851.2:c.495T= NP_062825.1:p.Tyr165=
NM_019851.3:c.495T= MANE Select NP_062825.1:p.Tyr165=