Canonical Allele Identifier: CA2579098527
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16993218-TGCG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993221_16993223del , CM000670.2:g.16993221_16993223del GRCh38
NC_000008.10:g.16850730_16850732del , CM000670.1:g.16850730_16850732del GRCh37
NC_000008.9:g.16895101_16895103del NCBI36
NG_015978.1:g.13945_13947del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.487_489del MANE Select ENSP00000180166.5:p.Arg163del
ENST00000180166.5:c.487_489del ENSP00000180166.5:p.Arg163del
ENST00000519941.1:c.191_193del
NM_019851.2:c.487_489del NP_062825.1:p.Arg163del
NM_019851.3:c.487_489del MANE Select NP_062825.1:p.Arg163del
Search 100 bp 5'
Search 100 bp 3'