Canonical Allele Identifier: CA1111331286
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v3: 8-16992603-G-GTTTT
gnomAD v4: 8-16992603-G-GTTTT
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992611_16992614dup , CM000670.2:g.16992611_16992614dup GRCh38
NC_000008.10:g.16850120_16850123dup , CM000670.1:g.16850120_16850123dup GRCh37
NC_000008.9:g.16894491_16894494dup NCBI36
NG_015978.1:g.14559_14562dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*465_*468dup MANE Select ENSP00000180166.5:n.*465_*468dup
ENST00000180166.5:c.*465_*468dup ENSP00000180166.5:n.*465_*468dup
NM_019851.3:c.*465_*468dup MANE Select NP_062825.1:n.*465_*468dup
Search 100 bp 5'
Search 100 bp 3'