Canonical Allele Identifier: CA377836928

Gene: FGF8

Linked Data

• dbSNP Id: rs2065068189
• MyVariant Identifiers: chr10:g.103534585G>A (hg19) ; chr10:g.101774828G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774828G>A , CM000672.2:g.101774828G>A	GRCh38
NC_000010.10:g.103534585G>A , CM000672.1:g.103534585G>A	GRCh37
NC_000010.9:g.103524575G>A	NCBI36
NG_007151.1:g.6243C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.241C>T MANE Select	ENSP00000321797.2:p.Arg81Trp
ENST00000618991.5:c.-72C>T	ENSP00000484420.1:n.-72C>T
ENST00000344255.8:c.208C>T	ENSP00000340039.3:p.Arg70Trp
ENST00000320185.6:c.241C>T	ENSP00000321797.2:p.Arg81Trp
ENST00000344255.7:c.208C>T	ENSP00000340039.3:p.Arg70Trp
ENST00000346714.7:c.121C>T	ENSP00000344306.3:p.Arg41Trp
ENST00000347978.2:c.154C>T	ENSP00000321945.2:p.Arg52Trp
ENST00000469792.6:c.*205C>T	ENSP00000473299.1:n.*205C>T
ENST00000485728.1:n.117C>T
ENST00000618991.4:c.-72C>T	ENSP00000484420.1:n.-72C>T
NM_001206389.1:c.-72C>T	NP_001193318.1:n.-72C>T
NM_006119.4:c.154C>T	NP_006110.1:p.Arg52Trp
NM_033163.3:c.241C>T	NP_149353.1:p.Arg81Trp
NM_033164.3:c.208C>T	NP_149354.1:p.Arg70Trp
NM_033165.3:c.121C>T	NP_149355.1:p.Arg41Trp
XM_011539509.1:c.163C>T	XP_011537811.1:p.Arg55Trp
NM_006119.5:c.154C>T	NP_006110.1:p.Arg52Trp
NM_033163.4:c.241C>T	NP_149353.1:p.Arg81Trp
NM_033164.4:c.208C>T	NP_149354.1:p.Arg70Trp
NM_033165.4:c.121C>T	NP_149355.1:p.Arg41Trp
NM_001206389.2:c.-72C>T	NP_001193318.1:n.-72C>T
NM_006119.6:c.154C>T	NP_006110.1:p.Arg52Trp
NM_033163.5:c.241C>T MANE Select	NP_149353.1:p.Arg81Trp
NM_033165.5:c.121C>T	NP_149355.1:p.Arg41Trp