Canonical Allele Identifier: CA370394449

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850723T>C (hg19) ; chr8:g.16993214T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993214T>C , CM000670.2:g.16993214T>C	GRCh38
NC_000008.10:g.16850723T>C , CM000670.1:g.16850723T>C	GRCh37
NC_000008.9:g.16895094T>C	NCBI36
NG_015978.1:g.13952A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.494A>G MANE Select	ENSP00000180166.5:p.Tyr165Cys
ENST00000180166.5:c.494A>G	ENSP00000180166.5:p.Tyr165Cys
ENST00000519941.1:c.198A>G
NM_019851.2:c.494A>G	NP_062825.1:p.Tyr165Cys
NM_019851.3:c.494A>G MANE Select	NP_062825.1:p.Tyr165Cys