Canonical Allele Identifier: CA2779223999
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992763G>C , CM000670.2:g.16992763G>C GRCh38
NC_000008.10:g.16850272G>C , CM000670.1:g.16850272G>C GRCh37
NC_000008.9:g.16894643G>C NCBI36
NG_015978.1:g.14403C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*309C>G MANE Select ENSP00000180166.5:n.*309C>G
ENST00000180166.5:c.*309C>G ENSP00000180166.5:n.*309C>G
NM_019851.3:c.*309C>G MANE Select NP_062825.1:n.*309C>G
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