Canonical Allele Identifier: CA459633938
Gene: FGF20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.16850710A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993201A>T , CM000670.2:g.16993201A>T GRCh38
NC_000008.10:g.16850710A>T , CM000670.1:g.16850710A>T GRCh37
NC_000008.9:g.16895081A>T NCBI36
NG_015978.1:g.13965T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.507T>A MANE Select ENSP00000180166.5:p.Leu169=
ENST00000180166.5:c.507T>A ENSP00000180166.5:p.Leu169=
ENST00000519941.1:c.211T>A
NM_019851.2:c.507T>A NP_062825.1:p.Leu169=
NM_019851.3:c.507T>A MANE Select NP_062825.1:p.Leu169=
Search 100 bp 5'
Search 100 bp 3'