Canonical Allele Identifier: CA470996197

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531307C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771550C>G , CM000672.2:g.101771550C>G	GRCh38
NC_000010.10:g.103531307C>G , CM000672.1:g.103531307C>G	GRCh37
NC_000010.9:g.103521297C>G	NCBI36
NG_007151.1:g.9521G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.357G>C MANE Select	ENSP00000321797.2:p.Thr119=
ENST00000618991.5:c.45G>C	ENSP00000484420.1:p.Thr15=
ENST00000344255.8:c.324G>C	ENSP00000340039.3:p.Thr108=
ENST00000320185.6:c.357G>C	ENSP00000321797.2:p.Thr119=
ENST00000344255.7:c.324G>C	ENSP00000340039.3:p.Thr108=
ENST00000346714.7:c.237G>C	ENSP00000344306.3:p.Thr79=
ENST00000347978.2:c.270G>C	ENSP00000321945.2:p.Thr90=
ENST00000469792.6:c.*321G>C	ENSP00000473299.1:n.*321G>C
ENST00000485728.1:n.233G>C
ENST00000618991.4:c.45G>C	ENSP00000484420.1:p.Thr15=
NM_001206389.1:c.45G>C	NP_001193318.1:p.Thr15=
NM_006119.4:c.270G>C	NP_006110.1:p.Thr90=
NM_033163.3:c.357G>C	NP_149353.1:p.Thr119=
NM_033164.3:c.324G>C	NP_149354.1:p.Thr108=
NM_033165.3:c.237G>C	NP_149355.1:p.Thr79=
XM_011539509.1:c.279G>C	XP_011537811.1:p.Thr93=
XR_946251.1:n.331C>G
XR_946252.1:n.262C>G
XR_946253.1:n.260C>G
XR_946252.2:n.352C>G
XR_946253.2:n.350C>G
NM_006119.5:c.270G>C	NP_006110.1:p.Thr90=
NM_033163.4:c.357G>C	NP_149353.1:p.Thr119=
NM_033164.4:c.324G>C	NP_149354.1:p.Thr108=
NM_033165.4:c.237G>C	NP_149355.1:p.Thr79=
NM_001206389.2:c.45G>C	NP_001193318.1:p.Thr15=
NM_006119.6:c.270G>C	NP_006110.1:p.Thr90=
NM_033163.5:c.357G>C MANE Select	NP_149353.1:p.Thr119=
NM_033165.5:c.237G>C	NP_149355.1:p.Thr79=