Canonical Allele Identifier: CA1767395668
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992826T= , CM000670.2:g.16992826T= GRCh38
NC_000008.10:g.16850335T= , CM000670.1:g.16850335T= GRCh37
NC_000008.9:g.16894706T= NCBI36
NG_015978.1:g.14340A=

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*246A= MANE Select ENSP00000180166.5:n.*246A=
ENST00000180166.5:c.*246A= ENSP00000180166.5:n.*246A=
NM_019851.2:c.*246A= NP_062825.1:n.*246A=
NM_019851.3:c.*246A= MANE Select NP_062825.1:n.*246A=