Canonical Allele Identifier: CA459634028

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850740T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993231T>G , CM000670.2:g.16993231T>G	GRCh38
NC_000008.10:g.16850740T>G , CM000670.1:g.16850740T>G	GRCh37
NC_000008.9:g.16895111T>G	NCBI36
NG_015978.1:g.13935A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.477A>C MANE Select	ENSP00000180166.5:p.Gly159=
ENST00000180166.5:c.477A>C	ENSP00000180166.5:p.Gly159=
ENST00000519941.1:c.181A>C
NM_019851.2:c.477A>C	NP_062825.1:p.Gly159=
NM_019851.3:c.477A>C MANE Select	NP_062825.1:p.Gly159=