Canonical Allele Identifier: CA470996294

Gene: FGF8

Linked Data

• gnomAD v4: 10-101774766-G-T
• MyVariant Identifiers: chr10:g.103534523G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774766G>T , CM000672.2:g.101774766G>T	GRCh38
NC_000010.10:g.103534523G>T , CM000672.1:g.103534523G>T	GRCh37
NC_000010.9:g.103524513G>T	NCBI36
NG_007151.1:g.6305C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.303C>A MANE Select	ENSP00000321797.2:p.Arg101=
ENST00000618991.5:c.-10C>A	ENSP00000484420.1:n.-10C>A
ENST00000344255.8:c.270C>A	ENSP00000340039.3:p.Arg90=
ENST00000320185.6:c.303C>A	ENSP00000321797.2:p.Arg101=
ENST00000344255.7:c.270C>A	ENSP00000340039.3:p.Arg90=
ENST00000346714.7:c.183C>A	ENSP00000344306.3:p.Arg61=
ENST00000347978.2:c.216C>A	ENSP00000321945.2:p.Arg72=
ENST00000469792.6:c.*267C>A	ENSP00000473299.1:n.*267C>A
ENST00000485728.1:n.179C>A
ENST00000618991.4:c.-10C>A	ENSP00000484420.1:n.-10C>A
NM_001206389.1:c.-10C>A	NP_001193318.1:n.-10C>A
NM_006119.4:c.216C>A	NP_006110.1:p.Arg72=
NM_033163.3:c.303C>A	NP_149353.1:p.Arg101=
NM_033164.3:c.270C>A	NP_149354.1:p.Arg90=
NM_033165.3:c.183C>A	NP_149355.1:p.Arg61=
XM_011539509.1:c.225C>A	XP_011537811.1:p.Arg75=
NM_006119.5:c.216C>A	NP_006110.1:p.Arg72=
NM_033163.4:c.303C>A	NP_149353.1:p.Arg101=
NM_033164.4:c.270C>A	NP_149354.1:p.Arg90=
NM_033165.4:c.183C>A	NP_149355.1:p.Arg61=
NM_001206389.2:c.-10C>A	NP_001193318.1:n.-10C>A
NM_006119.6:c.216C>A	NP_006110.1:p.Arg72=
NM_033163.5:c.303C>A MANE Select	NP_149353.1:p.Arg101=
NM_033165.5:c.183C>A	NP_149355.1:p.Arg61=