Canonical Allele Identifier: CA1111331313
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809946996
gnomAD v3: 8-16992885-AT-A
gnomAD v4: 8-16992885-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992886del , CM000670.2:g.16992886del GRCh38
NC_000008.10:g.16850395del , CM000670.1:g.16850395del GRCh37
NC_000008.9:g.16894766del NCBI36
NG_015978.1:g.14280del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*186del MANE Select ENSP00000180166.5:n.*186del
ENST00000180166.5:c.*186del ENSP00000180166.5:n.*186del
NM_019851.2:c.*186del NP_062825.1:n.*186del
NM_019851.3:c.*186del MANE Select NP_062825.1:n.*186del
Search 100 bp 5'
Search 100 bp 3'