Canonical Allele Identifier: CA370394441
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16993211-A-C
MyVariant Identifiers: chr8:g.16850720A>C (hg19) chr8:g.16993211A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993211A>C , CM000670.2:g.16993211A>C GRCh38
NC_000008.10:g.16850720A>C , CM000670.1:g.16850720A>C GRCh37
NC_000008.9:g.16895091A>C NCBI36
NG_015978.1:g.13955T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.497T>G MANE Select ENSP00000180166.5:p.Phe166Cys
ENST00000180166.5:c.497T>G ENSP00000180166.5:p.Phe166Cys
ENST00000519941.1:c.201T>G
NM_019851.2:c.497T>G NP_062825.1:p.Phe166Cys
NM_019851.3:c.497T>G MANE Select NP_062825.1:p.Phe166Cys
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