Canonical Allele Identifier: CA370394452
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.493T>C MANE Select ENSP00000180166.5:p.Tyr165His
ENST00000180166.5:c.493T>C ENSP00000180166.5:p.Tyr165His
ENST00000519941.1:c.197T>C
NM_019851.2:c.493T>C NP_062825.1:p.Tyr165His
NM_019851.3:c.493T>C MANE Select NP_062825.1:p.Tyr165His