Canonical Allele Identifier: CA370394269

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850638T>A (hg19) ; chr8:g.16993129T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993129T>A , CM000670.2:g.16993129T>A	GRCh38
NC_000008.10:g.16850638T>A , CM000670.1:g.16850638T>A	GRCh37
NC_000008.9:g.16895009T>A	NCBI36
NG_015978.1:g.14037A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.579A>T MANE Select	ENSP00000180166.5:p.Arg193Ser
ENST00000180166.5:c.579A>T	ENSP00000180166.5:p.Arg193Ser
ENST00000519941.1:c.283A>T
NM_019851.2:c.579A>T	NP_062825.1:p.Arg193Ser
NM_019851.3:c.579A>T MANE Select	NP_062825.1:p.Arg193Ser