Canonical Allele Identifier: CA1767396234
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993205G= , CM000670.2:g.16993205G= GRCh38
NC_000008.10:g.16850714G= , CM000670.1:g.16850714G= GRCh37
NC_000008.9:g.16895085G= NCBI36
NG_015978.1:g.13961C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.503C= MANE Select ENSP00000180166.5:p.Ala168=
ENST00000180166.5:c.503C= ENSP00000180166.5:p.Ala168=
ENST00000519941.1:c.207C=
NM_019851.2:c.503C= NP_062825.1:p.Ala168=
NM_019851.3:c.503C= MANE Select NP_062825.1:p.Ala168=
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