Canonical Allele Identifier: CA1767395339
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809935111
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992433del , CM000670.2:g.16992433del GRCh38
NC_000008.10:g.16849942del , CM000670.1:g.16849942del GRCh37
NC_000008.9:g.16894313del NCBI36
NG_015978.1:g.14738del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*644del MANE Select ENSP00000180166.5:n.*644del
ENST00000180166.5:c.*644del ENSP00000180166.5:n.*644del
NM_019851.3:c.*644del MANE Select NP_062825.1:n.*644del
Search 100 bp 5'
Search 100 bp 3'