Canonical Allele Identifier: CA470996095

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531292G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771535G>A , CM000672.2:g.101771535G>A	GRCh38
NC_000010.10:g.103531292G>A , CM000672.1:g.103531292G>A	GRCh37
NC_000010.9:g.103521282G>A	NCBI36
NG_007151.1:g.9536C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.372C>T MANE Select	ENSP00000321797.2:p.Ser124=
ENST00000618991.5:c.60C>T	ENSP00000484420.1:p.Ser20=
ENST00000344255.8:c.339C>T	ENSP00000340039.3:p.Ser113=
ENST00000320185.6:c.372C>T	ENSP00000321797.2:p.Ser124=
ENST00000344255.7:c.339C>T	ENSP00000340039.3:p.Ser113=
ENST00000346714.7:c.252C>T	ENSP00000344306.3:p.Ser84=
ENST00000347978.2:c.285C>T	ENSP00000321945.2:p.Ser95=
ENST00000469792.6:c.*336C>T	ENSP00000473299.1:n.*336C>T
ENST00000485728.1:n.248C>T
ENST00000618991.4:c.60C>T	ENSP00000484420.1:p.Ser20=
NM_001206389.1:c.60C>T	NP_001193318.1:p.Ser20=
NM_006119.4:c.285C>T	NP_006110.1:p.Ser95=
NM_033163.3:c.372C>T	NP_149353.1:p.Ser124=
NM_033164.3:c.339C>T	NP_149354.1:p.Ser113=
NM_033165.3:c.252C>T	NP_149355.1:p.Ser84=
XM_011539509.1:c.294C>T	XP_011537811.1:p.Ser98=
XR_946251.1:n.316G>A
XR_946252.1:n.247G>A
XR_946253.1:n.245G>A
XR_946252.2:n.337G>A
XR_946253.2:n.335G>A
NM_006119.5:c.285C>T	NP_006110.1:p.Ser95=
NM_033163.4:c.372C>T	NP_149353.1:p.Ser124=
NM_033164.4:c.339C>T	NP_149354.1:p.Ser113=
NM_033165.4:c.252C>T	NP_149355.1:p.Ser84=
NM_001206389.2:c.60C>T	NP_001193318.1:p.Ser20=
NM_006119.6:c.285C>T	NP_006110.1:p.Ser95=
NM_033163.5:c.372C>T MANE Select	NP_149353.1:p.Ser124=
NM_033165.5:c.252C>T	NP_149355.1:p.Ser84=