Canonical Allele Identifier: CA470996325

Gene: FGF8

Linked Data

• dbSNP Id: rs1564632353
• MyVariant Identifiers: chr10:g.103534574T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774817T>C , CM000672.2:g.101774817T>C	GRCh38
NC_000010.10:g.103534574T>C , CM000672.1:g.103534574T>C	GRCh37
NC_000010.9:g.103524564T>C	NCBI36
NG_007151.1:g.6254A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.252A>G MANE Select	ENSP00000321797.2:p.Gln84=
ENST00000618991.5:c.-61A>G	ENSP00000484420.1:n.-61A>G
ENST00000344255.8:c.219A>G	ENSP00000340039.3:p.Gln73=
ENST00000320185.6:c.252A>G	ENSP00000321797.2:p.Gln84=
ENST00000344255.7:c.219A>G	ENSP00000340039.3:p.Gln73=
ENST00000346714.7:c.132A>G	ENSP00000344306.3:p.Gln44=
ENST00000347978.2:c.165A>G	ENSP00000321945.2:p.Gln55=
ENST00000469792.6:c.*216A>G	ENSP00000473299.1:n.*216A>G
ENST00000485728.1:n.128A>G
ENST00000618991.4:c.-61A>G	ENSP00000484420.1:n.-61A>G
NM_001206389.1:c.-61A>G	NP_001193318.1:n.-61A>G
NM_006119.4:c.165A>G	NP_006110.1:p.Gln55=
NM_033163.3:c.252A>G	NP_149353.1:p.Gln84=
NM_033164.3:c.219A>G	NP_149354.1:p.Gln73=
NM_033165.3:c.132A>G	NP_149355.1:p.Gln44=
XM_011539509.1:c.174A>G	XP_011537811.1:p.Gln58=
NM_006119.5:c.165A>G	NP_006110.1:p.Gln55=
NM_033163.4:c.252A>G	NP_149353.1:p.Gln84=
NM_033164.4:c.219A>G	NP_149354.1:p.Gln73=
NM_033165.4:c.132A>G	NP_149355.1:p.Gln44=
NM_001206389.2:c.-61A>G	NP_001193318.1:n.-61A>G
NM_006119.6:c.165A>G	NP_006110.1:p.Gln55=
NM_033163.5:c.252A>G MANE Select	NP_149353.1:p.Gln84=
NM_033165.5:c.132A>G	NP_149355.1:p.Gln44=