Canonical Allele Identifier: CA1111331291
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v3: 8-16992616-TTAAAACA-T
gnomAD v4: 8-16992616-TTAAAACA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992619_16992625del , CM000670.2:g.16992619_16992625del GRCh38
NC_000008.10:g.16850128_16850134del , CM000670.1:g.16850128_16850134del GRCh37
NC_000008.9:g.16894499_16894505del NCBI36
NG_015978.1:g.14543_14549del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*449_*455del MANE Select ENSP00000180166.5:n.*449_*455del
ENST00000180166.5:c.*449_*455del ENSP00000180166.5:n.*449_*455del
NM_019851.3:c.*449_*455del MANE Select NP_062825.1:n.*449_*455del
Search 100 bp 5'
Search 100 bp 3'