Canonical Allele Identifier: CA1767395647
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992781_16992782delinsGT , CM000670.2:g.16992781_16992782delinsGT GRCh38
NC_000008.10:g.16850290_16850291delinsGT , CM000670.1:g.16850290_16850291delinsGT GRCh37
NC_000008.9:g.16894661_16894662delinsGT NCBI36
NG_015978.1:g.14384_14385delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*290_*291delinsAC MANE Select ENSP00000180166.5:n.*290_*291delinsAC
ENST00000180166.5:c.*290_*291delinsAC ENSP00000180166.5:n.*290_*291delinsAC
NM_019851.3:c.*290_*291delinsAC MANE Select NP_062825.1:n.*290_*291delinsAC
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