Canonical Allele Identifier: CA580052391
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs750613452
gnomAD v2: 8-16850112-G-GTTTTTTTTT
gnomAD v3: 8-16992603-G-GTTTTTTTTT
gnomAD v4: 8-16992603-G-GTTTTTTTTT
MyVariant Identifiers: chr8:g.16850113_16850114insTTTTTTTTT (hg19) chr8:g.16992604_16992605insTTTTTTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992606_16992614dup , CM000670.2:g.16992606_16992614dup GRCh38
NC_000008.10:g.16850115_16850123dup , CM000670.1:g.16850115_16850123dup GRCh37
NC_000008.9:g.16894486_16894494dup NCBI36
NG_015978.1:g.14554_14562dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*460_*468dup MANE Select ENSP00000180166.5:n.*460_*468dup
ENST00000180166.5:c.*460_*468dup ENSP00000180166.5:n.*460_*468dup
NM_019851.3:c.*460_*468dup MANE Select NP_062825.1:n.*460_*468dup
Search 100 bp 5'
Search 100 bp 3'