Canonical Allele Identifier: CA5657663
Gene: FGF8 HGNC NCBI

Linked Data

dbSNP Id: rs184500788

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774846G>A , CM000672.2:g.101774846G>A GRCh38
NC_000010.10:g.103534603G>A , CM000672.1:g.103534603G>A GRCh37
NC_000010.9:g.103524593G>A NCBI36
NG_007151.1:g.6225C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.223C>T MANE Select ENSP00000321797.2:p.Leu75Phe
ENST00000618991.5:c.-90C>T ENSP00000484420.1:n.-90C>T
ENST00000344255.8:c.190C>T ENSP00000340039.3:p.Leu64Phe
ENST00000320185.6:c.223C>T ENSP00000321797.2:p.Leu75Phe
ENST00000344255.7:c.190C>T ENSP00000340039.3:p.Leu64Phe
ENST00000346714.7:c.103C>T ENSP00000344306.3:p.Leu35Phe
ENST00000347978.2:c.136C>T ENSP00000321945.2:p.Leu46Phe
ENST00000469792.6:c.*187C>T ENSP00000473299.1:n.*187C>T
ENST00000485728.1:n.99C>T
ENST00000618991.4:c.-90C>T ENSP00000484420.1:n.-90C>T
NM_001206389.1:c.-90C>T NP_001193318.1:n.-90C>T
NM_006119.4:c.136C>T NP_006110.1:p.Leu46Phe
NM_033163.3:c.223C>T NP_149353.1:p.Leu75Phe
NM_033164.3:c.190C>T NP_149354.1:p.Leu64Phe
NM_033165.3:c.103C>T NP_149355.1:p.Leu35Phe
XM_011539509.1:c.145C>T XP_011537811.1:p.Leu49Phe
NM_006119.5:c.136C>T NP_006110.1:p.Leu46Phe
NM_033163.4:c.223C>T NP_149353.1:p.Leu75Phe
NM_033164.4:c.190C>T NP_149354.1:p.Leu64Phe
NM_033165.4:c.103C>T NP_149355.1:p.Leu35Phe
NM_001206389.2:c.-90C>T NP_001193318.1:n.-90C>T
NM_006119.6:c.136C>T NP_006110.1:p.Leu46Phe
NM_033163.5:c.223C>T MANE Select NP_149353.1:p.Leu75Phe
NM_033165.5:c.103C>T NP_149355.1:p.Leu35Phe