Canonical Allele Identifier: CA470996318

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534559G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774802G>C , CM000672.2:g.101774802G>C	GRCh38
NC_000010.10:g.103534559G>C , CM000672.1:g.103534559G>C	GRCh37
NC_000010.9:g.103524549G>C	NCBI36
NG_007151.1:g.6269C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.267C>G MANE Select	ENSP00000321797.2:p.Thr89=
ENST00000618991.5:c.-46C>G	ENSP00000484420.1:n.-46C>G
ENST00000344255.8:c.234C>G	ENSP00000340039.3:p.Thr78=
ENST00000320185.6:c.267C>G	ENSP00000321797.2:p.Thr89=
ENST00000344255.7:c.234C>G	ENSP00000340039.3:p.Thr78=
ENST00000346714.7:c.147C>G	ENSP00000344306.3:p.Thr49=
ENST00000347978.2:c.180C>G	ENSP00000321945.2:p.Thr60=
ENST00000469792.6:c.*231C>G	ENSP00000473299.1:n.*231C>G
ENST00000485728.1:n.143C>G
ENST00000618991.4:c.-46C>G	ENSP00000484420.1:n.-46C>G
NM_001206389.1:c.-46C>G	NP_001193318.1:n.-46C>G
NM_006119.4:c.180C>G	NP_006110.1:p.Thr60=
NM_033163.3:c.267C>G	NP_149353.1:p.Thr89=
NM_033164.3:c.234C>G	NP_149354.1:p.Thr78=
NM_033165.3:c.147C>G	NP_149355.1:p.Thr49=
XM_011539509.1:c.189C>G	XP_011537811.1:p.Thr63=
NM_006119.5:c.180C>G	NP_006110.1:p.Thr60=
NM_033163.4:c.267C>G	NP_149353.1:p.Thr89=
NM_033164.4:c.234C>G	NP_149354.1:p.Thr78=
NM_033165.4:c.147C>G	NP_149355.1:p.Thr49=
NM_001206389.2:c.-46C>G	NP_001193318.1:n.-46C>G
NM_006119.6:c.180C>G	NP_006110.1:p.Thr60=
NM_033163.5:c.267C>G MANE Select	NP_149353.1:p.Thr89=
NM_033165.5:c.147C>G	NP_149355.1:p.Thr49=