Canonical Allele Identifier: CA1767395850
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992931A= , CM000670.2:g.16992931A= GRCh38
NC_000008.10:g.16850440A= , CM000670.1:g.16850440A= GRCh37
NC_000008.9:g.16894811A= NCBI36
NG_015978.1:g.14235T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*141T= MANE Select ENSP00000180166.5:n.*141T=
ENST00000180166.5:c.*141T= ENSP00000180166.5:n.*141T=
NM_019851.2:c.*141T= NP_062825.1:n.*141T=
NM_019851.3:c.*141T= MANE Select NP_062825.1:n.*141T=
Search 100 bp 5'
Search 100 bp 3'