Canonical Allele Identifier: CA370394429

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850714G>T (hg19) ; chr8:g.16993205G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993205G>T , CM000670.2:g.16993205G>T	GRCh38
NC_000008.10:g.16850714G>T , CM000670.1:g.16850714G>T	GRCh37
NC_000008.9:g.16895085G>T	NCBI36
NG_015978.1:g.13961C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.503C>A MANE Select	ENSP00000180166.5:p.Ala168Glu
ENST00000180166.5:c.503C>A	ENSP00000180166.5:p.Ala168Glu
ENST00000519941.1:c.207C>A
NM_019851.2:c.503C>A	NP_062825.1:p.Ala168Glu
NM_019851.3:c.503C>A MANE Select	NP_062825.1:p.Ala168Glu