Canonical Allele Identifier: CA377836998

Gene: FGF8

Linked Data

• gnomAD v4: 10-101774839-C-T
• MyVariant Identifiers: chr10:g.103534596C>T (hg19) ; chr10:g.101774839C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774839C>T , CM000672.2:g.101774839C>T	GRCh38
NC_000010.10:g.103534596C>T , CM000672.1:g.103534596C>T	GRCh37
NC_000010.9:g.103524586C>T	NCBI36
NG_007151.1:g.6232G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000320185.7:c.230G>A MANE Select	ENSP00000321797.2:p.Arg77His
ENST00000618991.5:c.-83G>A	ENSP00000484420.1:n.-83G>A
ENST00000344255.8:c.197G>A	ENSP00000340039.3:p.Arg66His
ENST00000320185.6:c.230G>A	ENSP00000321797.2:p.Arg77His
ENST00000344255.7:c.197G>A	ENSP00000340039.3:p.Arg66His
ENST00000346714.7:c.110G>A	ENSP00000344306.3:p.Arg37His
ENST00000347978.2:c.143G>A	ENSP00000321945.2:p.Arg48His
ENST00000469792.6:c.*194G>A	ENSP00000473299.1:n.*194G>A
ENST00000485728.1:n.106G>A
ENST00000618991.4:c.-83G>A	ENSP00000484420.1:n.-83G>A
NM_001206389.1:c.-83G>A	NP_001193318.1:n.-83G>A
NM_006119.4:c.143G>A	NP_006110.1:p.Arg48His
NM_033163.3:c.230G>A	NP_149353.1:p.Arg77His
NM_033164.3:c.197G>A	NP_149354.1:p.Arg66His
NM_033165.3:c.110G>A	NP_149355.1:p.Arg37His
XM_011539509.1:c.152G>A	XP_011537811.1:p.Arg51His
NM_006119.5:c.143G>A	NP_006110.1:p.Arg48His
NM_033163.4:c.230G>A	NP_149353.1:p.Arg77His
NM_033164.4:c.197G>A	NP_149354.1:p.Arg66His
NM_033165.4:c.110G>A	NP_149355.1:p.Arg37His
NM_001206389.2:c.-83G>A	NP_001193318.1:n.-83G>A
NM_006119.6:c.143G>A	NP_006110.1:p.Arg48His
NM_033163.5:c.230G>A MANE Select	NP_149353.1:p.Arg77His
NM_033165.5:c.110G>A	NP_149355.1:p.Arg37His