Canonical Allele Identifier: CA2686252555
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16993225-A-AT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993225_16993226insT , CM000670.2:g.16993225_16993226insT GRCh38
NC_000008.10:g.16850734_16850735insT , CM000670.1:g.16850734_16850735insT GRCh37
NC_000008.9:g.16895105_16895106insT NCBI36
NG_015978.1:g.13940_13941insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.482_483insA MANE Select ENSP00000180166.5:p.Gly162TrpfsTer9
ENST00000180166.5:c.482_483insA ENSP00000180166.5:p.Gly162TrpfsTer9
ENST00000519941.1:c.186_187insA
NM_019851.2:c.482_483insA NP_062825.1:p.Gly162TrpfsTer9
NM_019851.3:c.482_483insA MANE Select NP_062825.1:p.Gly162TrpfsTer9
Search 100 bp 5'
Search 100 bp 3'