Canonical Allele Identifier: CA4641578
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs759071753
ExAC: 8:16850720 A / G
gnomAD v2: 8-16850720-A-G
gnomAD v4: 8-16993211-A-G
MyVariant Identifiers: chr8:g.16850720A>G (hg19) chr8:g.16993211A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.497T>C MANE Select ENSP00000180166.5:p.Phe166Ser
ENST00000180166.5:c.497T>C ENSP00000180166.5:p.Phe166Ser
ENST00000519941.1:c.201T>C
NM_019851.2:c.497T>C NP_062825.1:p.Phe166Ser
NM_019851.3:c.497T>C MANE Select NP_062825.1:p.Phe166Ser
Search 100 bp 5'
Search 100 bp 3'