Canonical Allele Identifier: CA377837132
Gene: FGF8 HGNC NCBI

Linked Data

dbSNP Id: rs1474057032

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774854G>A , CM000672.2:g.101774854G>A GRCh38
NC_000010.10:g.103534611G>A , CM000672.1:g.103534611G>A GRCh37
NC_000010.9:g.103524601G>A NCBI36
NG_007151.1:g.6217C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.215C>T MANE Select ENSP00000321797.2:p.Thr72Met
ENST00000618991.5:c.-98C>T ENSP00000484420.1:n.-98C>T
ENST00000344255.8:c.182C>T ENSP00000340039.3:p.Thr61Met
ENST00000320185.6:c.215C>T ENSP00000321797.2:p.Thr72Met
ENST00000344255.7:c.182C>T ENSP00000340039.3:p.Thr61Met
ENST00000346714.7:c.95C>T ENSP00000344306.3:p.Thr32Met
ENST00000347978.2:c.128C>T ENSP00000321945.2:p.Thr43Met
ENST00000469792.6:c.*179C>T ENSP00000473299.1:n.*179C>T
ENST00000485728.1:n.91C>T
ENST00000618991.4:c.-98C>T ENSP00000484420.1:n.-98C>T
NM_001206389.1:c.-98C>T NP_001193318.1:n.-98C>T
NM_006119.4:c.128C>T NP_006110.1:p.Thr43Met
NM_033163.3:c.215C>T NP_149353.1:p.Thr72Met
NM_033164.3:c.182C>T NP_149354.1:p.Thr61Met
NM_033165.3:c.95C>T NP_149355.1:p.Thr32Met
XM_011539509.1:c.137C>T XP_011537811.1:p.Thr46Met
NM_006119.5:c.128C>T NP_006110.1:p.Thr43Met
NM_033163.4:c.215C>T NP_149353.1:p.Thr72Met
NM_033164.4:c.182C>T NP_149354.1:p.Thr61Met
NM_033165.4:c.95C>T NP_149355.1:p.Thr32Met
NM_001206389.2:c.-98C>T NP_001193318.1:n.-98C>T
NM_006119.6:c.128C>T NP_006110.1:p.Thr43Met
NM_033163.5:c.215C>T MANE Select NP_149353.1:p.Thr72Met
NM_033165.5:c.95C>T NP_149355.1:p.Thr32Met