Canonical Allele Identifier: CA1767395783
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992901A= , CM000670.2:g.16992901A= GRCh38
NC_000008.10:g.16850410A= , CM000670.1:g.16850410A= GRCh37
NC_000008.9:g.16894781A= NCBI36
NG_015978.1:g.14265T=

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*171T= MANE Select ENSP00000180166.5:n.*171T=
ENST00000180166.5:c.*171T= ENSP00000180166.5:n.*171T=
NM_019851.2:c.*171T= NP_062825.1:n.*171T=
NM_019851.3:c.*171T= MANE Select NP_062825.1:n.*171T=