Canonical Allele Identifier: CA370394419
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993200T>C , CM000670.2:g.16993200T>C GRCh38
NC_000008.10:g.16850709T>C , CM000670.1:g.16850709T>C GRCh37
NC_000008.9:g.16895080T>C NCBI36
NG_015978.1:g.13966A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.508A>G MANE Select ENSP00000180166.5:p.Asn170Asp
ENST00000180166.5:c.508A>G ENSP00000180166.5:p.Asn170Asp
ENST00000519941.1:c.212A>G
NM_019851.2:c.508A>G NP_062825.1:p.Asn170Asp
NM_019851.3:c.508A>G MANE Select NP_062825.1:p.Asn170Asp