Canonical Allele Identifier: CA1980746912
Gene: FGF3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69818779G= , CM000673.2:g.69818779G= GRCh38
NC_000011.9:g.69633547G= , CM000673.1:g.69633547G= GRCh37
NC_000011.8:g.69342484G= NCBI36
NG_009016.1:g.5646C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.155C= MANE Select ENSP00000334122.2:p.Thr52=
ENST00000334134.2:c.155C= ENSP00000334122.2:p.Thr52=
NM_005247.2:c.155C= NP_005238.1:p.Thr52=
NM_005247.3:c.155C= NP_005238.1:p.Thr52=
NM_005247.4:c.155C= MANE Select NP_005238.1:p.Thr52=
Search 100 bp 5'
Search 100 bp 3'