Canonical Allele Identifier: CA370394453
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993215A>C , CM000670.2:g.16993215A>C GRCh38
NC_000008.10:g.16850724A>C , CM000670.1:g.16850724A>C GRCh37
NC_000008.9:g.16895095A>C NCBI36
NG_015978.1:g.13951T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.493T>G MANE Select ENSP00000180166.5:p.Tyr165Asp
ENST00000180166.5:c.493T>G ENSP00000180166.5:p.Tyr165Asp
ENST00000519941.1:c.197T>G
NM_019851.2:c.493T>G NP_062825.1:p.Tyr165Asp
NM_019851.3:c.493T>G MANE Select NP_062825.1:p.Tyr165Asp