Canonical Allele Identifier: CA470996327

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534580G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774823G>A , CM000672.2:g.101774823G>A	GRCh38
NC_000010.10:g.103534580G>A , CM000672.1:g.103534580G>A	GRCh37
NC_000010.9:g.103524570G>A	NCBI36
NG_007151.1:g.6248C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.246C>T MANE Select	ENSP00000321797.2:p.Thr82=
ENST00000618991.5:c.-67C>T	ENSP00000484420.1:n.-67C>T
ENST00000344255.8:c.213C>T	ENSP00000340039.3:p.Thr71=
ENST00000320185.6:c.246C>T	ENSP00000321797.2:p.Thr82=
ENST00000344255.7:c.213C>T	ENSP00000340039.3:p.Thr71=
ENST00000346714.7:c.126C>T	ENSP00000344306.3:p.Thr42=
ENST00000347978.2:c.159C>T	ENSP00000321945.2:p.Thr53=
ENST00000469792.6:c.*210C>T	ENSP00000473299.1:n.*210C>T
ENST00000485728.1:n.122C>T
ENST00000618991.4:c.-67C>T	ENSP00000484420.1:n.-67C>T
NM_001206389.1:c.-67C>T	NP_001193318.1:n.-67C>T
NM_006119.4:c.159C>T	NP_006110.1:p.Thr53=
NM_033163.3:c.246C>T	NP_149353.1:p.Thr82=
NM_033164.3:c.213C>T	NP_149354.1:p.Thr71=
NM_033165.3:c.126C>T	NP_149355.1:p.Thr42=
XM_011539509.1:c.168C>T	XP_011537811.1:p.Thr56=
NM_006119.5:c.159C>T	NP_006110.1:p.Thr53=
NM_033163.4:c.246C>T	NP_149353.1:p.Thr82=
NM_033164.4:c.213C>T	NP_149354.1:p.Thr71=
NM_033165.4:c.126C>T	NP_149355.1:p.Thr42=
NM_001206389.2:c.-67C>T	NP_001193318.1:n.-67C>T
NM_006119.6:c.159C>T	NP_006110.1:p.Thr53=
NM_033163.5:c.246C>T MANE Select	NP_149353.1:p.Thr82=
NM_033165.5:c.126C>T	NP_149355.1:p.Thr42=