Canonical Allele Identifier: CA2779224018
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992992T>C , CM000670.2:g.16992992T>C GRCh38
NC_000008.10:g.16850501T>C , CM000670.1:g.16850501T>C GRCh37
NC_000008.9:g.16894872T>C NCBI36
NG_015978.1:g.14174A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*80A>G MANE Select ENSP00000180166.5:n.*80A>G
ENST00000180166.5:c.*80A>G ENSP00000180166.5:n.*80A>G
ENST00000519941.1:c.420A>G
NM_019851.2:c.*80A>G NP_062825.1:n.*80A>G
NM_019851.3:c.*80A>G MANE Select NP_062825.1:n.*80A>G
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