Canonical Allele Identifier: CA1111331280
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809939408
gnomAD v3: 8-16992594-T-G
gnomAD v4: 8-16992594-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992594T>G , CM000670.2:g.16992594T>G GRCh38
NC_000008.10:g.16850103T>G , CM000670.1:g.16850103T>G GRCh37
NC_000008.9:g.16894474T>G NCBI36
NG_015978.1:g.14572A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*478A>C MANE Select ENSP00000180166.5:n.*478A>C
ENST00000180166.5:c.*478A>C ENSP00000180166.5:n.*478A>C
NM_019851.3:c.*478A>C MANE Select NP_062825.1:n.*478A>C
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