Canonical Allele Identifier: CA475468078

Gene: FGF3

Linked Data

• MyVariant Identifiers: chr11:g.69625300T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69810532T>G , CM000673.2:g.69810532T>G	GRCh38
NC_000011.9:g.69625300T>G , CM000673.1:g.69625300T>G	GRCh37
NC_000011.8:g.69334481T>G	NCBI36
NG_009016.1:g.13893A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334134.4:c.493A>C MANE Select	ENSP00000334122.2:p.Arg165=
ENST00000646078.1:n.340A>C
ENST00000334134.2:c.493A>C	ENSP00000334122.2:p.Arg165=
NM_005247.2:c.493A>C	NP_005238.1:p.Arg165=
NM_005247.3:c.493A>C	NP_005238.1:p.Arg165=
NM_005247.4:c.493A>C MANE Select	NP_005238.1:p.Arg165=