Canonical Allele Identifier: CA377836964

Gene: FGF8

Linked Data

• dbSNP Id: rs866334037
• MyVariant Identifiers: chr10:g.103534590A>C (hg19) ; chr10:g.101774833A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774833A>C , CM000672.2:g.101774833A>C	GRCh38
NC_000010.10:g.103534590A>C , CM000672.1:g.103534590A>C	GRCh37
NC_000010.9:g.103524580A>C	NCBI36
NG_007151.1:g.6238T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.236T>G MANE Select	ENSP00000321797.2:p.Leu79Arg
ENST00000618991.5:c.-77T>G	ENSP00000484420.1:n.-77T>G
ENST00000344255.8:c.203T>G	ENSP00000340039.3:p.Leu68Arg
ENST00000320185.6:c.236T>G	ENSP00000321797.2:p.Leu79Arg
ENST00000344255.7:c.203T>G	ENSP00000340039.3:p.Leu68Arg
ENST00000346714.7:c.116T>G	ENSP00000344306.3:p.Leu39Arg
ENST00000347978.2:c.149T>G	ENSP00000321945.2:p.Leu50Arg
ENST00000469792.6:c.*200T>G	ENSP00000473299.1:n.*200T>G
ENST00000485728.1:n.112T>G
ENST00000618991.4:c.-77T>G	ENSP00000484420.1:n.-77T>G
NM_001206389.1:c.-77T>G	NP_001193318.1:n.-77T>G
NM_006119.4:c.149T>G	NP_006110.1:p.Leu50Arg
NM_033163.3:c.236T>G	NP_149353.1:p.Leu79Arg
NM_033164.3:c.203T>G	NP_149354.1:p.Leu68Arg
NM_033165.3:c.116T>G	NP_149355.1:p.Leu39Arg
XM_011539509.1:c.158T>G	XP_011537811.1:p.Leu53Arg
NM_006119.5:c.149T>G	NP_006110.1:p.Leu50Arg
NM_033163.4:c.236T>G	NP_149353.1:p.Leu79Arg
NM_033164.4:c.203T>G	NP_149354.1:p.Leu68Arg
NM_033165.4:c.116T>G	NP_149355.1:p.Leu39Arg
NM_001206389.2:c.-77T>G	NP_001193318.1:n.-77T>G
NM_006119.6:c.149T>G	NP_006110.1:p.Leu50Arg
NM_033163.5:c.236T>G MANE Select	NP_149353.1:p.Leu79Arg
NM_033165.5:c.116T>G	NP_149355.1:p.Leu39Arg