Canonical Allele Identifier: CA1767395861
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992961A= , CM000670.2:g.16992961A= GRCh38
NC_000008.10:g.16850470A= , CM000670.1:g.16850470A= GRCh37
NC_000008.9:g.16894841A= NCBI36
NG_015978.1:g.14205T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*111T= MANE Select ENSP00000180166.5:n.*111T=
ENST00000180166.5:c.*111T= ENSP00000180166.5:n.*111T=
NM_019851.2:c.*111T= NP_062825.1:n.*111T=
NM_019851.3:c.*111T= MANE Select NP_062825.1:n.*111T=
Search 100 bp 5'
Search 100 bp 3'