Canonical Allele Identifier: CA1111331282
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1000399884
gnomAD v3: 8-16992602-A-T
gnomAD v4: 8-16992602-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992602A>T , CM000670.2:g.16992602A>T GRCh38
NC_000008.10:g.16850111A>T , CM000670.1:g.16850111A>T GRCh37
NC_000008.9:g.16894482A>T NCBI36
NG_015978.1:g.14564T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*470T>A MANE Select ENSP00000180166.5:n.*470T>A
ENST00000180166.5:c.*470T>A ENSP00000180166.5:n.*470T>A
NM_019851.3:c.*470T>A MANE Select NP_062825.1:n.*470T>A
Search 100 bp 5'
Search 100 bp 3'