Canonical Allele Identifier: CA370394349
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993164T>C , CM000670.2:g.16993164T>C GRCh38
NC_000008.10:g.16850673T>C , CM000670.1:g.16850673T>C GRCh37
NC_000008.9:g.16895044T>C NCBI36
NG_015978.1:g.14002A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.544A>G MANE Select ENSP00000180166.5:p.Lys182Glu
ENST00000180166.5:c.544A>G ENSP00000180166.5:p.Lys182Glu
ENST00000519941.1:c.248A>G
NM_019851.2:c.544A>G NP_062825.1:p.Lys182Glu
NM_019851.3:c.544A>G MANE Select NP_062825.1:p.Lys182Glu