Canonical Allele Identifier: CA370394287
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16993138-G-C
MyVariant Identifiers: chr8:g.16850647G>C (hg19) chr8:g.16993138G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993138G>C , CM000670.2:g.16993138G>C GRCh38
NC_000008.10:g.16850647G>C , CM000670.1:g.16850647G>C GRCh37
NC_000008.9:g.16895018G>C NCBI36
NG_015978.1:g.14028C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.570C>G MANE Select ENSP00000180166.5:p.Phe190Leu
ENST00000180166.5:c.570C>G ENSP00000180166.5:p.Phe190Leu
ENST00000519941.1:c.274C>G
NM_019851.2:c.570C>G NP_062825.1:p.Phe190Leu
NM_019851.3:c.570C>G MANE Select NP_062825.1:p.Phe190Leu
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