Canonical Allele Identifier: CA377834394

Gene: FGF8

Linked Data

• dbSNP Id: rs1589810695
• MyVariant Identifiers: chr10:g.103531267T>C (hg19) ; chr10:g.101771510T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771510T>C , CM000672.2:g.101771510T>C	GRCh38
NC_000010.10:g.103531267T>C , CM000672.1:g.103531267T>C	GRCh37
NC_000010.9:g.103521257T>C	NCBI36
NG_007151.1:g.9561A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.397A>G MANE Select	ENSP00000321797.2:p.Thr133Ala
ENST00000618991.5:c.85A>G	ENSP00000484420.1:p.Thr29Ala
ENST00000344255.8:c.364A>G	ENSP00000340039.3:p.Thr122Ala
ENST00000320185.6:c.397A>G	ENSP00000321797.2:p.Thr133Ala
ENST00000344255.7:c.364A>G	ENSP00000340039.3:p.Thr122Ala
ENST00000346714.7:c.277A>G	ENSP00000344306.3:p.Thr93Ala
ENST00000347978.2:c.310A>G	ENSP00000321945.2:p.Thr104Ala
ENST00000469792.6:c.*361A>G	ENSP00000473299.1:n.*361A>G
ENST00000485728.1:n.273A>G
ENST00000618991.4:c.85A>G	ENSP00000484420.1:p.Thr29Ala
NM_001206389.1:c.85A>G	NP_001193318.1:p.Thr29Ala
NM_006119.4:c.310A>G	NP_006110.1:p.Thr104Ala
NM_033163.3:c.397A>G	NP_149353.1:p.Thr133Ala
NM_033164.3:c.364A>G	NP_149354.1:p.Thr122Ala
NM_033165.3:c.277A>G	NP_149355.1:p.Thr93Ala
XM_011539509.1:c.319A>G	XP_011537811.1:p.Thr107Ala
XR_946251.1:n.291T>C
XR_946252.1:n.222T>C
XR_946253.1:n.220T>C
XR_946252.2:n.312T>C
XR_946253.2:n.310T>C
NM_006119.5:c.310A>G	NP_006110.1:p.Thr104Ala
NM_033163.4:c.397A>G	NP_149353.1:p.Thr133Ala
NM_033164.4:c.364A>G	NP_149354.1:p.Thr122Ala
NM_033165.4:c.277A>G	NP_149355.1:p.Thr93Ala
NM_001206389.2:c.85A>G	NP_001193318.1:p.Thr29Ala
NM_006119.6:c.310A>G	NP_006110.1:p.Thr104Ala
NM_033163.5:c.397A>G MANE Select	NP_149353.1:p.Thr133Ala
NM_033165.5:c.277A>G	NP_149355.1:p.Thr93Ala