Canonical Allele Identifier: CA459633937

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850710A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.507T>C MANE Select	ENSP00000180166.5:p.Leu169=
ENST00000180166.5:c.507T>C	ENSP00000180166.5:p.Leu169=
ENST00000519941.1:c.211T>C
NM_019851.2:c.507T>C	NP_062825.1:p.Leu169=
NM_019851.3:c.507T>C MANE Select	NP_062825.1:p.Leu169=