Canonical Allele Identifier: CA370394481

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850741C>A (hg19) ; chr8:g.16993232C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993232C>A , CM000670.2:g.16993232C>A	GRCh38
NC_000008.10:g.16850741C>A , CM000670.1:g.16850741C>A	GRCh37
NC_000008.9:g.16895112C>A	NCBI36
NG_015978.1:g.13934G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.476G>T MANE Select	ENSP00000180166.5:p.Gly159Val
ENST00000180166.5:c.476G>T	ENSP00000180166.5:p.Gly159Val
ENST00000519941.1:c.180G>T
NM_019851.2:c.476G>T	NP_062825.1:p.Gly159Val
NM_019851.3:c.476G>T MANE Select	NP_062825.1:p.Gly159Val