Canonical Allele Identifier: CA5657662

Gene: FGF8

Linked Data

• dbSNP Id: rs777079870
• ExAC: 10:103534588 T / C
• gnomAD v2: 10-103534588-T-C
• gnomAD v4: 10-101774831-T-C
• MyVariant Identifiers: chr10:g.103534588T>C (hg19) ; chr10:g.101774831T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774831T>C , CM000672.2:g.101774831T>C	GRCh38
NC_000010.10:g.103534588T>C , CM000672.1:g.103534588T>C	GRCh37
NC_000010.9:g.103524578T>C	NCBI36
NG_007151.1:g.6240A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.238A>G MANE Select	ENSP00000321797.2:p.Ile80Val
ENST00000618991.5:c.-75A>G	ENSP00000484420.1:n.-75A>G
ENST00000344255.8:c.205A>G	ENSP00000340039.3:p.Ile69Val
ENST00000320185.6:c.238A>G	ENSP00000321797.2:p.Ile80Val
ENST00000344255.7:c.205A>G	ENSP00000340039.3:p.Ile69Val
ENST00000346714.7:c.118A>G	ENSP00000344306.3:p.Ile40Val
ENST00000347978.2:c.151A>G	ENSP00000321945.2:p.Ile51Val
ENST00000469792.6:c.*202A>G	ENSP00000473299.1:n.*202A>G
ENST00000485728.1:n.114A>G
ENST00000618991.4:c.-75A>G	ENSP00000484420.1:n.-75A>G
NM_001206389.1:c.-75A>G	NP_001193318.1:n.-75A>G
NM_006119.4:c.151A>G	NP_006110.1:p.Ile51Val
NM_033163.3:c.238A>G	NP_149353.1:p.Ile80Val
NM_033164.3:c.205A>G	NP_149354.1:p.Ile69Val
NM_033165.3:c.118A>G	NP_149355.1:p.Ile40Val
XM_011539509.1:c.160A>G	XP_011537811.1:p.Ile54Val
NM_006119.5:c.151A>G	NP_006110.1:p.Ile51Val
NM_033163.4:c.238A>G	NP_149353.1:p.Ile80Val
NM_033164.4:c.205A>G	NP_149354.1:p.Ile69Val
NM_033165.4:c.118A>G	NP_149355.1:p.Ile40Val
NM_001206389.2:c.-75A>G	NP_001193318.1:n.-75A>G
NM_006119.6:c.151A>G	NP_006110.1:p.Ile51Val
NM_033163.5:c.238A>G MANE Select	NP_149353.1:p.Ile80Val
NM_033165.5:c.118A>G	NP_149355.1:p.Ile40Val