Canonical Allele Identifier: CA1980746907
Gene: FGF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69818757G= , CM000673.2:g.69818757G= GRCh38
NC_000011.9:g.69633525G= , CM000673.1:g.69633525G= GRCh37
NC_000011.8:g.69342462G= NCBI36
NG_009016.1:g.5668C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.177C= MANE Select ENSP00000334122.2:p.His59=
ENST00000334134.2:c.177C= ENSP00000334122.2:p.His59=
NM_005247.2:c.177C= NP_005238.1:p.His59=
NM_005247.3:c.177C= NP_005238.1:p.His59=
NM_005247.4:c.177C= MANE Select NP_005238.1:p.His59=