Canonical Allele Identifier: CA1980742069
Gene: FGF3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69810530C= , CM000673.2:g.69810530C= GRCh38
NC_000011.9:g.69625298C= , CM000673.1:g.69625298C= GRCh37
NC_000011.8:g.69334479C= NCBI36
NG_009016.1:g.13895G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.495G= MANE Select ENSP00000334122.2:p.Arg165=
ENST00000646078.1:n.342G=
ENST00000334134.2:c.495G= ENSP00000334122.2:p.Arg165=
NM_005247.2:c.495G= NP_005238.1:p.Arg165=
NM_005247.3:c.495G= NP_005238.1:p.Arg165=
NM_005247.4:c.495G= MANE Select NP_005238.1:p.Arg165=
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