Canonical Allele Identifier: CA1111331330
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v3: 8-16992998-A-ACAC
gnomAD v4: 8-16992998-A-ACAC
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992998_16992999insCAC , CM000670.2:g.16992998_16992999insCAC GRCh38
NC_000008.10:g.16850507_16850508insCAC , CM000670.1:g.16850507_16850508insCAC GRCh37
NC_000008.9:g.16894878_16894879insCAC NCBI36
NG_015978.1:g.14167_14168insGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*73_*74insGTG MANE Select ENSP00000180166.5:n.*73_*74insGTG
ENST00000180166.5:c.*73_*74insGTG ENSP00000180166.5:n.*73_*74insGTG
ENST00000519941.1:c.413_414insGTG
NM_019851.2:c.*73_*74insGTG NP_062825.1:n.*73_*74insGTG
NM_019851.3:c.*73_*74insGTG MANE Select NP_062825.1:n.*73_*74insGTG
Search 100 bp 5'
Search 100 bp 3'