Canonical Allele Identifier: CA1767395324
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992414_16992415delinsCG , CM000670.2:g.16992414_16992415delinsCG GRCh38
NC_000008.10:g.16849923_16849924delinsCG , CM000670.1:g.16849923_16849924delinsCG GRCh37
NC_000008.9:g.16894294_16894295delinsCG NCBI36
NG_015978.1:g.14751_14752delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*657_*658delinsCG MANE Select ENSP00000180166.5:n.*657_*658delinsCG
ENST00000180166.5:c.*657_*658delinsCG ENSP00000180166.5:n.*657_*658delinsCG
NM_019851.3:c.*657_*658delinsCG MANE Select NP_062825.1:n.*657_*658delinsCG
Search 100 bp 5'
Search 100 bp 3'