Canonical Allele Identifier: CA377834494

Gene: FGF8

Linked Data

• dbSNP Id: rs1213544634
• gnomAD v2: 10-103531297-C-T
• gnomAD v4: 10-101771540-C-T
• MyVariant Identifiers: chr10:g.103531297C>T (hg19) ; chr10:g.101771540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771540C>T , CM000672.2:g.101771540C>T	GRCh38
NC_000010.10:g.103531297C>T , CM000672.1:g.103531297C>T	GRCh37
NC_000010.9:g.103521287C>T	NCBI36
NG_007151.1:g.9531G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.367G>A MANE Select	ENSP00000321797.2:p.Gly123Arg
ENST00000618991.5:c.55G>A	ENSP00000484420.1:p.Gly19Arg
ENST00000344255.8:c.334G>A	ENSP00000340039.3:p.Gly112Arg
ENST00000320185.6:c.367G>A	ENSP00000321797.2:p.Gly123Arg
ENST00000344255.7:c.334G>A	ENSP00000340039.3:p.Gly112Arg
ENST00000346714.7:c.247G>A	ENSP00000344306.3:p.Gly83Arg
ENST00000347978.2:c.280G>A	ENSP00000321945.2:p.Gly94Arg
ENST00000469792.6:c.*331G>A	ENSP00000473299.1:n.*331G>A
ENST00000485728.1:n.243G>A
ENST00000618991.4:c.55G>A	ENSP00000484420.1:p.Gly19Arg
NM_001206389.1:c.55G>A	NP_001193318.1:p.Gly19Arg
NM_006119.4:c.280G>A	NP_006110.1:p.Gly94Arg
NM_033163.3:c.367G>A	NP_149353.1:p.Gly123Arg
NM_033164.3:c.334G>A	NP_149354.1:p.Gly112Arg
NM_033165.3:c.247G>A	NP_149355.1:p.Gly83Arg
XM_011539509.1:c.289G>A	XP_011537811.1:p.Gly97Arg
XR_946251.1:n.321C>T
XR_946252.1:n.252C>T
XR_946253.1:n.250C>T
XR_946252.2:n.342C>T
XR_946253.2:n.340C>T
NM_006119.5:c.280G>A	NP_006110.1:p.Gly94Arg
NM_033163.4:c.367G>A	NP_149353.1:p.Gly123Arg
NM_033164.4:c.334G>A	NP_149354.1:p.Gly112Arg
NM_033165.4:c.247G>A	NP_149355.1:p.Gly83Arg
NM_001206389.2:c.55G>A	NP_001193318.1:p.Gly19Arg
NM_006119.6:c.280G>A	NP_006110.1:p.Gly94Arg
NM_033163.5:c.367G>A MANE Select	NP_149353.1:p.Gly123Arg
NM_033165.5:c.247G>A	NP_149355.1:p.Gly83Arg