Canonical Allele Identifier: CA370394356
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs749155129

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993168C>A , CM000670.2:g.16993168C>A GRCh38
NC_000008.10:g.16850677C>A , CM000670.1:g.16850677C>A GRCh37
NC_000008.9:g.16895048C>A NCBI36
NG_015978.1:g.13998G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.540G>T MANE Select ENSP00000180166.5:p.Arg180Ser
ENST00000180166.5:c.540G>T ENSP00000180166.5:p.Arg180Ser
ENST00000519941.1:c.244G>T
NM_019851.2:c.540G>T NP_062825.1:p.Arg180Ser
NM_019851.3:c.540G>T MANE Select NP_062825.1:p.Arg180Ser