Canonical Allele Identifier: CA1767395378
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992473T= , CM000670.2:g.16992473T= GRCh38
NC_000008.10:g.16849982T= , CM000670.1:g.16849982T= GRCh37
NC_000008.9:g.16894353T= NCBI36
NG_015978.1:g.14693A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*599A= MANE Select ENSP00000180166.5:n.*599A=
ENST00000180166.5:c.*599A= ENSP00000180166.5:n.*599A=
NM_019851.3:c.*599A= MANE Select NP_062825.1:n.*599A=