Canonical Allele Identifier: CA1980742047

Gene: FGF3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69810484G= , CM000673.2:g.69810484G=	GRCh38
NC_000011.9:g.69625252G= , CM000673.1:g.69625252G=	GRCh37
NC_000011.8:g.69334433G=	NCBI36
NG_009016.1:g.13941C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334134.4:c.541C= MANE Select	ENSP00000334122.2:p.Arg181=
ENST00000646078.1:n.388C=
ENST00000334134.2:c.541C=	ENSP00000334122.2:p.Arg181=
NM_005247.2:c.541C=	NP_005238.1:p.Arg181=
NM_005247.3:c.541C=	NP_005238.1:p.Arg181=
NM_005247.4:c.541C= MANE Select	NP_005238.1:p.Arg181=