Canonical Allele Identifier: CA1767395381
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992477T= , CM000670.2:g.16992477T= GRCh38
NC_000008.10:g.16849986T= , CM000670.1:g.16849986T= GRCh37
NC_000008.9:g.16894357T= NCBI36
NG_015978.1:g.14689A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*595A= MANE Select ENSP00000180166.5:n.*595A=
ENST00000180166.5:c.*595A= ENSP00000180166.5:n.*595A=
NM_019851.3:c.*595A= MANE Select NP_062825.1:n.*595A=