Canonical Allele Identifier: CA459633946

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850716C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993207C>A , CM000670.2:g.16993207C>A	GRCh38
NC_000008.10:g.16850716C>A , CM000670.1:g.16850716C>A	GRCh37
NC_000008.9:g.16895087C>A	NCBI36
NG_015978.1:g.13959G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.501G>T MANE Select	ENSP00000180166.5:p.Val167=
ENST00000180166.5:c.501G>T	ENSP00000180166.5:p.Val167=
ENST00000519941.1:c.205G>T
NM_019851.2:c.501G>T	NP_062825.1:p.Val167=
NM_019851.3:c.501G>T MANE Select	NP_062825.1:p.Val167=