Canonical Allele Identifier: CA1767395374
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992471A= , CM000670.2:g.16992471A= GRCh38
NC_000008.10:g.16849980A= , CM000670.1:g.16849980A= GRCh37
NC_000008.9:g.16894351A= NCBI36
NG_015978.1:g.14695T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*601T= MANE Select ENSP00000180166.5:n.*601T=
ENST00000180166.5:c.*601T= ENSP00000180166.5:n.*601T=
NM_019851.3:c.*601T= MANE Select NP_062825.1:n.*601T=