Canonical Allele Identifier: CA1932376991
Gene: FGF8 HGNC NCBI

Linked Data

dbSNP Id: rs2065070468

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101775021G>C , CM000672.2:g.101775021G>C GRCh38
NC_000010.10:g.103534778G>C , CM000672.1:g.103534778G>C GRCh37
NC_000010.9:g.103524768G>C NCBI36
NG_007151.1:g.6050C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.157-109C>G MANE Select ENSP00000321797.2:n.157-109C>G
ENST00000618991.5:c.-123-142C>G ENSP00000484420.1:n.-123-142C>G
ENST00000344255.8:c.156+109C>G ENSP00000340039.3:n.156+109C>G
ENST00000320185.6:c.157-109C>G ENSP00000321797.2:n.157-109C>G
ENST00000344255.7:c.156+109C>G ENSP00000340039.3:n.156+109C>G
ENST00000346714.7:c.70-142C>G ENSP00000344306.3:n.70-142C>G
ENST00000347978.2:c.70-109C>G ENSP00000321945.2:n.70-109C>G
ENST00000469792.6:c.*154-142C>G ENSP00000473299.1:n.*154-142C>G
ENST00000485728.1:n.33-109C>G
ENST00000618991.4:c.-123-142C>G ENSP00000484420.1:n.-123-142C>G
NM_001206389.1:c.-123-142C>G NP_001193318.1:n.-123-142C>G
NM_006119.4:c.70-109C>G NP_006110.1:n.70-109C>G
NM_033163.3:c.157-109C>G NP_149353.1:n.157-109C>G
NM_033164.3:c.156+109C>G NP_149354.1:n.156+109C>G
NM_033165.3:c.70-142C>G NP_149355.1:n.70-142C>G
XM_011539509.1:c.79-109C>G XP_011537811.1:n.79-109C>G
NM_006119.5:c.70-109C>G NP_006110.1:n.70-109C>G
NM_033163.4:c.157-109C>G NP_149353.1:n.157-109C>G
NM_033164.4:c.156+109C>G NP_149354.1:n.156+109C>G
NM_033165.4:c.70-142C>G NP_149355.1:n.70-142C>G
NM_001206389.2:c.-123-142C>G NP_001193318.1:n.-123-142C>G
NM_006119.6:c.70-109C>G NP_006110.1:n.70-109C>G
NM_033163.5:c.157-109C>G MANE Select NP_149353.1:n.157-109C>G
NM_033165.5:c.70-142C>G NP_149355.1:n.70-142C>G