Canonical Allele Identifier: CA470996352

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534613C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774856C>T , CM000672.2:g.101774856C>T	GRCh38
NC_000010.10:g.103534613C>T , CM000672.1:g.103534613C>T	GRCh37
NC_000010.9:g.103524603C>T	NCBI36
NG_007151.1:g.6215G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.213G>A MANE Select	ENSP00000321797.2:p.Val71=
ENST00000618991.5:c.-100G>A	ENSP00000484420.1:n.-100G>A
ENST00000344255.8:c.180G>A	ENSP00000340039.3:p.Val60=
ENST00000320185.6:c.213G>A	ENSP00000321797.2:p.Val71=
ENST00000344255.7:c.180G>A	ENSP00000340039.3:p.Val60=
ENST00000346714.7:c.93G>A	ENSP00000344306.3:p.Val31=
ENST00000347978.2:c.126G>A	ENSP00000321945.2:p.Val42=
ENST00000469792.6:c.*177G>A	ENSP00000473299.1:n.*177G>A
ENST00000485728.1:n.89G>A
ENST00000618991.4:c.-100G>A	ENSP00000484420.1:n.-100G>A
NM_001206389.1:c.-100G>A	NP_001193318.1:n.-100G>A
NM_006119.4:c.126G>A	NP_006110.1:p.Val42=
NM_033163.3:c.213G>A	NP_149353.1:p.Val71=
NM_033164.3:c.180G>A	NP_149354.1:p.Val60=
NM_033165.3:c.93G>A	NP_149355.1:p.Val31=
XM_011539509.1:c.135G>A	XP_011537811.1:p.Val45=
NM_006119.5:c.126G>A	NP_006110.1:p.Val42=
NM_033163.4:c.213G>A	NP_149353.1:p.Val71=
NM_033164.4:c.180G>A	NP_149354.1:p.Val60=
NM_033165.4:c.93G>A	NP_149355.1:p.Val31=
NM_001206389.2:c.-100G>A	NP_001193318.1:n.-100G>A
NM_006119.6:c.126G>A	NP_006110.1:p.Val42=
NM_033163.5:c.213G>A MANE Select	NP_149353.1:p.Val71=
NM_033165.5:c.93G>A	NP_149355.1:p.Val31=