Canonical Allele Identifier: CA172904173
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs921238581
gnomAD v4: 8-16993167-A-T
MyVariant Identifiers: chr8:g.16850676A>T (hg19) chr8:g.16993167A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993167A>T , CM000670.2:g.16993167A>T GRCh38
NC_000008.10:g.16850676A>T , CM000670.1:g.16850676A>T GRCh37
NC_000008.9:g.16895047A>T NCBI36
NG_015978.1:g.13999T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.541T>A MANE Select ENSP00000180166.5:p.Ser181Thr
ENST00000180166.5:c.541T>A ENSP00000180166.5:p.Ser181Thr
ENST00000519941.1:c.245T>A
NM_019851.2:c.541T>A NP_062825.1:p.Ser181Thr
NM_019851.3:c.541T>A MANE Select NP_062825.1:p.Ser181Thr
Search 100 bp 5'
Search 100 bp 3'