Canonical Allele Identifier: CA172903486
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs535500971
gnomAD v3: 8-16992656-C-A
gnomAD v4: 8-16992656-C-A
MyVariant Identifiers: chr8:g.16850165C>A (hg19) chr8:g.16992656C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992656C>A , CM000670.2:g.16992656C>A GRCh38
NC_000008.10:g.16850165C>A , CM000670.1:g.16850165C>A GRCh37
NC_000008.9:g.16894536C>A NCBI36
NG_015978.1:g.14510G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*416G>T MANE Select ENSP00000180166.5:n.*416G>T
ENST00000180166.5:c.*416G>T ENSP00000180166.5:n.*416G>T
NM_019851.3:c.*416G>T MANE Select NP_062825.1:n.*416G>T
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