Canonical Allele Identifier: CA4641555
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs761133332
ExAC: 8:16850635 T / C
gnomAD v2: 8-16850635-T-C
gnomAD v4: 8-16993126-T-C
MyVariant Identifiers: chr8:g.16850635T>C (hg19) chr8:g.16993126T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993126T>C , CM000670.2:g.16993126T>C GRCh38
NC_000008.10:g.16850635T>C , CM000670.1:g.16850635T>C GRCh37
NC_000008.9:g.16895006T>C NCBI36
NG_015978.1:g.14040A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.582A>G MANE Select ENSP00000180166.5:p.Pro194=
ENST00000180166.5:c.582A>G ENSP00000180166.5:p.Pro194=
ENST00000519941.1:c.286A>G
NM_019851.2:c.582A>G NP_062825.1:p.Pro194=
NM_019851.3:c.582A>G MANE Select NP_062825.1:p.Pro194=
Search 100 bp 5'
Search 100 bp 3'