Canonical Allele Identifier: CA470996183

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531301G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771544G>A , CM000672.2:g.101771544G>A	GRCh38
NC_000010.10:g.103531301G>A , CM000672.1:g.103531301G>A	GRCh37
NC_000010.9:g.103521291G>A	NCBI36
NG_007151.1:g.9527C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.363C>T MANE Select	ENSP00000321797.2:p.Thr121=
ENST00000618991.5:c.51C>T	ENSP00000484420.1:p.Thr17=
ENST00000344255.8:c.330C>T	ENSP00000340039.3:p.Thr110=
ENST00000320185.6:c.363C>T	ENSP00000321797.2:p.Thr121=
ENST00000344255.7:c.330C>T	ENSP00000340039.3:p.Thr110=
ENST00000346714.7:c.243C>T	ENSP00000344306.3:p.Thr81=
ENST00000347978.2:c.276C>T	ENSP00000321945.2:p.Thr92=
ENST00000469792.6:c.*327C>T	ENSP00000473299.1:n.*327C>T
ENST00000485728.1:n.239C>T
ENST00000618991.4:c.51C>T	ENSP00000484420.1:p.Thr17=
NM_001206389.1:c.51C>T	NP_001193318.1:p.Thr17=
NM_006119.4:c.276C>T	NP_006110.1:p.Thr92=
NM_033163.3:c.363C>T	NP_149353.1:p.Thr121=
NM_033164.3:c.330C>T	NP_149354.1:p.Thr110=
NM_033165.3:c.243C>T	NP_149355.1:p.Thr81=
XM_011539509.1:c.285C>T	XP_011537811.1:p.Thr95=
XR_946251.1:n.325G>A
XR_946252.1:n.256G>A
XR_946253.1:n.254G>A
XR_946252.2:n.346G>A
XR_946253.2:n.344G>A
NM_006119.5:c.276C>T	NP_006110.1:p.Thr92=
NM_033163.4:c.363C>T	NP_149353.1:p.Thr121=
NM_033164.4:c.330C>T	NP_149354.1:p.Thr110=
NM_033165.4:c.243C>T	NP_149355.1:p.Thr81=
NM_001206389.2:c.51C>T	NP_001193318.1:p.Thr17=
NM_006119.6:c.276C>T	NP_006110.1:p.Thr92=
NM_033163.5:c.363C>T MANE Select	NP_149353.1:p.Thr121=
NM_033165.5:c.243C>T	NP_149355.1:p.Thr81=