Canonical Allele Identifier: CA172903359
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs145080533
gnomAD v3: 8-16992543-A-G
gnomAD v4: 8-16992543-A-G
MyVariant Identifiers: chr8:g.16850052A>G (hg19) chr8:g.16992543A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992543A>G , CM000670.2:g.16992543A>G GRCh38
NC_000008.10:g.16850052A>G , CM000670.1:g.16850052A>G GRCh37
NC_000008.9:g.16894423A>G NCBI36
NG_015978.1:g.14623T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*529T>C MANE Select ENSP00000180166.5:n.*529T>C
ENST00000180166.5:c.*529T>C ENSP00000180166.5:n.*529T>C
NM_019851.3:c.*529T>C MANE Select NP_062825.1:n.*529T>C
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