Canonical Allele Identifier: CA459634013

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850728G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993219G>T , CM000670.2:g.16993219G>T	GRCh38
NC_000008.10:g.16850728G>T , CM000670.1:g.16850728G>T	GRCh37
NC_000008.9:g.16895099G>T	NCBI36
NG_015978.1:g.13947C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.489C>A MANE Select	ENSP00000180166.5:p.Arg163=
ENST00000180166.5:c.489C>A	ENSP00000180166.5:p.Arg163=
ENST00000519941.1:c.193C>A
NM_019851.2:c.489C>A	NP_062825.1:p.Arg163=
NM_019851.3:c.489C>A MANE Select	NP_062825.1:p.Arg163=