Canonical Allele Identifier: CA370394430
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993206C>A , CM000670.2:g.16993206C>A GRCh38
NC_000008.10:g.16850715C>A , CM000670.1:g.16850715C>A GRCh37
NC_000008.9:g.16895086C>A NCBI36
NG_015978.1:g.13960G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.502G>T MANE Select ENSP00000180166.5:p.Ala168Ser
ENST00000180166.5:c.502G>T ENSP00000180166.5:p.Ala168Ser
ENST00000519941.1:c.206G>T
NM_019851.2:c.502G>T NP_062825.1:p.Ala168Ser
NM_019851.3:c.502G>T MANE Select NP_062825.1:p.Ala168Ser