Canonical Allele Identifier: CA470996201

Gene: FGF8

Linked Data

• gnomAD v4: 10-101771553-C-T
• MyVariant Identifiers: chr10:g.103531310C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771553C>T , CM000672.2:g.101771553C>T	GRCh38
NC_000010.10:g.103531310C>T , CM000672.1:g.103531310C>T	GRCh37
NC_000010.9:g.103521300C>T	NCBI36
NG_007151.1:g.9518G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.354G>A MANE Select	ENSP00000321797.2:p.Glu118=
ENST00000618991.5:c.42G>A	ENSP00000484420.1:p.Glu14=
ENST00000344255.8:c.321G>A	ENSP00000340039.3:p.Glu107=
ENST00000320185.6:c.354G>A	ENSP00000321797.2:p.Glu118=
ENST00000344255.7:c.321G>A	ENSP00000340039.3:p.Glu107=
ENST00000346714.7:c.234G>A	ENSP00000344306.3:p.Glu78=
ENST00000347978.2:c.267G>A	ENSP00000321945.2:p.Glu89=
ENST00000469792.6:c.*318G>A	ENSP00000473299.1:n.*318G>A
ENST00000485728.1:n.230G>A
ENST00000618991.4:c.42G>A	ENSP00000484420.1:p.Glu14=
NM_001206389.1:c.42G>A	NP_001193318.1:p.Glu14=
NM_006119.4:c.267G>A	NP_006110.1:p.Glu89=
NM_033163.3:c.354G>A	NP_149353.1:p.Glu118=
NM_033164.3:c.321G>A	NP_149354.1:p.Glu107=
NM_033165.3:c.234G>A	NP_149355.1:p.Glu78=
XM_011539509.1:c.276G>A	XP_011537811.1:p.Glu92=
XR_946251.1:n.334C>T
XR_946252.1:n.265C>T
XR_946253.1:n.263C>T
XR_946252.2:n.355C>T
XR_946253.2:n.353C>T
NM_006119.5:c.267G>A	NP_006110.1:p.Glu89=
NM_033163.4:c.354G>A	NP_149353.1:p.Glu118=
NM_033164.4:c.321G>A	NP_149354.1:p.Glu107=
NM_033165.4:c.234G>A	NP_149355.1:p.Glu78=
NM_001206389.2:c.42G>A	NP_001193318.1:p.Glu14=
NM_006119.6:c.267G>A	NP_006110.1:p.Glu89=
NM_033163.5:c.354G>A MANE Select	NP_149353.1:p.Glu118=
NM_033165.5:c.234G>A	NP_149355.1:p.Glu78=