Canonical Allele Identifier: CA470996098

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531295T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771538T>G , CM000672.2:g.101771538T>G	GRCh38
NC_000010.10:g.103531295T>G , CM000672.1:g.103531295T>G	GRCh37
NC_000010.9:g.103521285T>G	NCBI36
NG_007151.1:g.9533A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000320185.7:c.369A>C MANE Select	ENSP00000321797.2:p.Gly123=
ENST00000618991.5:c.57A>C	ENSP00000484420.1:p.Gly19=
ENST00000344255.8:c.336A>C	ENSP00000340039.3:p.Gly112=
ENST00000320185.6:c.369A>C	ENSP00000321797.2:p.Gly123=
ENST00000344255.7:c.336A>C	ENSP00000340039.3:p.Gly112=
ENST00000346714.7:c.249A>C	ENSP00000344306.3:p.Gly83=
ENST00000347978.2:c.282A>C	ENSP00000321945.2:p.Gly94=
ENST00000469792.6:c.*333A>C	ENSP00000473299.1:n.*333A>C
ENST00000485728.1:n.245A>C
ENST00000618991.4:c.57A>C	ENSP00000484420.1:p.Gly19=
NM_001206389.1:c.57A>C	NP_001193318.1:p.Gly19=
NM_006119.4:c.282A>C	NP_006110.1:p.Gly94=
NM_033163.3:c.369A>C	NP_149353.1:p.Gly123=
NM_033164.3:c.336A>C	NP_149354.1:p.Gly112=
NM_033165.3:c.249A>C	NP_149355.1:p.Gly83=
XM_011539509.1:c.291A>C	XP_011537811.1:p.Gly97=
XR_946251.1:n.319T>G
XR_946252.1:n.250T>G
XR_946253.1:n.248T>G
XR_946252.2:n.340T>G
XR_946253.2:n.338T>G
NM_006119.5:c.282A>C	NP_006110.1:p.Gly94=
NM_033163.4:c.369A>C	NP_149353.1:p.Gly123=
NM_033164.4:c.336A>C	NP_149354.1:p.Gly112=
NM_033165.4:c.249A>C	NP_149355.1:p.Gly83=
NM_001206389.2:c.57A>C	NP_001193318.1:p.Gly19=
NM_006119.6:c.282A>C	NP_006110.1:p.Gly94=
NM_033163.5:c.369A>C MANE Select	NP_149353.1:p.Gly123=
NM_033165.5:c.249A>C	NP_149355.1:p.Gly83=