Canonical Allele Identifier: CA459633772
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1170334580
gnomAD v3: 8-16992908-AT-A
gnomAD v4: 8-16992908-AT-A
MyVariant Identifiers: chr8:g.16850418del (hg19) chr8:g.16992909del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992916del , CM000670.2:g.16992916del GRCh38
NC_000008.10:g.16850425del , CM000670.1:g.16850425del GRCh37
NC_000008.9:g.16894796del NCBI36
NG_015978.1:g.14257del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*163del MANE Select ENSP00000180166.5:n.*163del
ENST00000180166.5:c.*163del ENSP00000180166.5:n.*163del
NM_019851.2:c.*163del NP_062825.1:n.*163del
NM_019851.3:c.*163del MANE Select NP_062825.1:n.*163del
Search 100 bp 5'
Search 100 bp 3'