Canonical Allele Identifier: CA377834895

Gene: FGF8

Linked Data

• dbSNP Id: rs774503381
• gnomAD v2: 10-103531315-C-T
• gnomAD v4: 10-101771558-C-T
• MyVariant Identifiers: chr10:g.103531315C>T (hg19) ; chr10:g.101771558C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771558C>T , CM000672.2:g.101771558C>T	GRCh38
NC_000010.10:g.103531315C>T , CM000672.1:g.103531315C>T	GRCh37
NC_000010.9:g.103521305C>T	NCBI36
NG_007151.1:g.9513G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.349G>A MANE Select	ENSP00000321797.2:p.Val117Met
ENST00000618991.5:c.37G>A	ENSP00000484420.1:p.Val13Met
ENST00000344255.8:c.316G>A	ENSP00000340039.3:p.Val106Met
ENST00000320185.6:c.349G>A	ENSP00000321797.2:p.Val117Met
ENST00000344255.7:c.316G>A	ENSP00000340039.3:p.Val106Met
ENST00000346714.7:c.229G>A	ENSP00000344306.3:p.Val77Met
ENST00000347978.2:c.262G>A	ENSP00000321945.2:p.Val88Met
ENST00000469792.6:c.*313G>A	ENSP00000473299.1:n.*313G>A
ENST00000485728.1:n.225G>A
ENST00000618991.4:c.37G>A	ENSP00000484420.1:p.Val13Met
NM_001206389.1:c.37G>A	NP_001193318.1:p.Val13Met
NM_006119.4:c.262G>A	NP_006110.1:p.Val88Met
NM_033163.3:c.349G>A	NP_149353.1:p.Val117Met
NM_033164.3:c.316G>A	NP_149354.1:p.Val106Met
NM_033165.3:c.229G>A	NP_149355.1:p.Val77Met
XM_011539509.1:c.271G>A	XP_011537811.1:p.Val91Met
XR_946251.1:n.339C>T
XR_946252.1:n.270C>T
XR_946253.1:n.268C>T
XR_946252.2:n.360C>T
XR_946253.2:n.358C>T
NM_006119.5:c.262G>A	NP_006110.1:p.Val88Met
NM_033163.4:c.349G>A	NP_149353.1:p.Val117Met
NM_033164.4:c.316G>A	NP_149354.1:p.Val106Met
NM_033165.4:c.229G>A	NP_149355.1:p.Val77Met
NM_001206389.2:c.37G>A	NP_001193318.1:p.Val13Met
NM_006119.6:c.262G>A	NP_006110.1:p.Val88Met
NM_033163.5:c.349G>A MANE Select	NP_149353.1:p.Val117Met
NM_033165.5:c.229G>A	NP_149355.1:p.Val77Met