Canonical Allele Identifier: CA123000
Gene: FGFR2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13298
dbSNP Id: rs121918509

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121488095C>T , CM000672.2:g.121488095C>T GRCh38
NC_000010.10:g.123247609C>T , CM000672.1:g.123247609C>T GRCh37
NC_000010.9:g.123237599C>T NCBI36
NG_012449.1:g.115364G>A
NG_012449.2:g.115364G>A

Transcript Alleles

HGVS Amino-acid change
NM_000141.4:c.1882G>A VV NP_000132.3:p.Ala628Thr
NM_001144913.1:c.1885G>A VV NP_001138385.1:p.Ala629Thr
NM_001144914.1:c.1546G>A VV NP_001138386.1:p.Ala516Thr
NM_001144915.1:c.1615G>A VV NP_001138387.1:p.Ala539Thr
NM_001144916.1:c.1537G>A VV NP_001138388.1:p.Ala513Thr
NM_001144917.1:c.1534G>A VV NP_001138389.1:p.Ala512Thr
NM_001144918.1:c.1531G>A VV NP_001138390.1:p.Ala511Thr
NM_001144919.1:c.1618G>A VV NP_001138391.1:p.Ala540Thr
NM_022970.3:c.1885G>A VV NP_075259.4:p.Ala629Thr
NM_023029.2:c.1615G>A VV NP_075418.1:p.Ala539Thr
NR_073009.1:n.2332G>A
XM_006717708.2:c.1936G>A XP_006717771.1:p.Ala646Thr
XM_006717709.2:c.1933G>A XP_006717772.1:p.Ala645Thr
XM_006717710.2:c.1942G>A XP_006717773.1:p.Ala648Thr
XM_006717711.2:c.1675G>A XP_006717774.1:p.Ala559Thr
XM_006717712.2:c.1597G>A XP_006717775.1:p.Ala533Thr
XM_006717713.2:c.1939G>A XP_006717776.1:p.Ala647Thr
XM_011539510.1:c.1198G>A XP_011537812.1:p.Ala400Thr
NM_001320654.1:c.1198G>A VV NP_001307583.1:p.Ala400Thr
NM_001320658.1:c.1876G>A VV NP_001307587.1:p.Ala626Thr
XM_006717708.3:c.1936G>A XP_006717771.1:p.Ala646Thr
XM_006717710.4:c.1942G>A XP_006717773.1:p.Ala648Thr
XM_017015920.2:c.1936G>A XP_016871409.1:p.Ala646Thr
XM_017015921.2:c.1933G>A XP_016871410.1:p.Ala645Thr
XM_017015924.2:c.1594G>A XP_016871413.1:p.Ala532Thr
XM_017015925.2:c.1588G>A XP_016871414.1:p.Ala530Thr
XM_024447887.1:c.1672G>A XP_024303655.1:p.Ala558Thr
XM_024447888.1:c.1669G>A XP_024303656.1:p.Ala557Thr
XM_024447889.1:c.1666G>A XP_024303657.1:p.Ala556Thr
XM_024447890.1:c.1675G>A XP_024303658.1:p.Ala559Thr
XM_024447891.1:c.1597G>A XP_024303659.1:p.Ala533Thr
XM_024447892.1:c.712G>A XP_024303660.1:p.Ala238Thr
ENST00000336553.10:c.1609G>A ENSP00000337665.6:p.Ala537Thr
ENST00000346997.6:c.1876G>A ENSP00000263451.5:p.Ala626Thr
ENST00000351936.10:c.1882G>A ENSP00000309878.9:p.Ala628Thr
ENST00000356226.8:c.1531G>A ENSP00000348559.4:p.Ala511Thr
ENST00000357555.9:c.1615G>A ENSP00000350166.5:p.Ala539Thr
ENST00000358487.9:c.1882G>A ENSP00000351276.5:p.Ala628Thr
ENST00000360144.7:c.1618G>A ENSP00000353262.3:p.Ala540Thr
ENST00000369056.5:c.1885G>A ENSP00000358052.1:p.Ala629Thr
ENST00000369058.7:c.1885G>A ENSP00000358054.3:p.Ala629Thr
ENST00000369059.5:c.1540G>A ENSP00000358055.1:p.Ala514Thr
ENST00000369060.8:c.1534G>A ENSP00000358056.4:p.Ala512Thr
ENST00000369061.8:c.1546G>A ENSP00000358057.4:p.Ala516Thr
ENST00000429361.5:n.658G>A ENSP00000404219.1:p.Ala220Thr
ENST00000457416.6:c.1885G>A ENSP00000410294.2:p.Ala629Thr
ENST00000478859.5:c.1198G>A ENSP00000474011.1:p.Ala400Thr
ENST00000604236.5:c.*929G>A ENSP00000474109.1:p.=
ENST00000613048.4:c.1615G>A ENSP00000484154.1:p.Ala539Thr