Canonical Allele Identifier: CA370394259

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850633A>C (hg19) ; chr8:g.16993124A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993124A>C , CM000670.2:g.16993124A>C	GRCh38
NC_000008.10:g.16850633A>C , CM000670.1:g.16850633A>C	GRCh37
NC_000008.9:g.16895004A>C	NCBI36
NG_015978.1:g.14042T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.584T>G MANE Select	ENSP00000180166.5:p.Val195Gly
ENST00000180166.5:c.584T>G	ENSP00000180166.5:p.Val195Gly
ENST00000519941.1:c.288T>G
NM_019851.2:c.584T>G	NP_062825.1:p.Val195Gly
NM_019851.3:c.584T>G MANE Select	NP_062825.1:p.Val195Gly