Canonical Allele Identifier: CA16618939
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423481
ClinVar RCV Id: RCV000482209
dbSNP Id: rs1064796452
MyVariant Identifiers: chr10:g.123274776T>C (hg19) chr10:g.121515262T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121515262T>C , CM000672.2:g.121515262T>C GRCh38
NC_000010.10:g.123274776T>C , CM000672.1:g.123274776T>C GRCh37
NC_000010.9:g.123264766T>C NCBI36
NG_012449.1:g.88197A>G
NG_012449.2:g.88197A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.1145A>G MANE Plus Clinical ENSP00000410294.2:p.Tyr382Cys
ENST00000351936.11:c.1142A>G ENSP00000309878.10:p.Tyr381Cys
ENST00000638709.2:c.-29A>G ENSP00000491912.2:n.-29A>G
ENST00000682296.1:n.490A>G
ENST00000682550.1:c.797A>G ENSP00000507633.1:p.Tyr266Cys
ENST00000682772.1:c.-29A>G ENSP00000506848.1:n.-29A>G
ENST00000683211.1:c.1142A>G ENSP00000508257.1:p.Tyr381Cys
ENST00000683250.1:c.404-11321A>G ENSP00000506847.1:n.404-11321A>G
ENST00000683418.1:n.3489A>G
ENST00000684153.1:c.797A>G ENSP00000506937.1:p.Tyr266Cys
ENST00000358487.10:c.1142A>G MANE Select ENSP00000351276.6:p.Tyr381Cys
ENST00000336553.10:c.875A>G ENSP00000337665.6:p.Tyr292Cys
ENST00000346997.6:c.1142A>G ENSP00000263451.5:p.Tyr381Cys
ENST00000351936.10:c.1148A>G ENSP00000309878.9:p.Tyr383Cys
ENST00000356226.8:c.797A>G ENSP00000348559.4:p.Tyr266Cys
ENST00000357555.9:c.875A>G ENSP00000350166.5:p.Tyr292Cys
ENST00000358487.9:c.1142A>G ENSP00000351276.5:p.Tyr381Cys
ENST00000360144.7:c.878A>G ENSP00000353262.3:p.Tyr293Cys
ENST00000369056.5:c.1145A>G ENSP00000358052.1:p.Tyr382Cys
ENST00000369058.7:c.1145A>G ENSP00000358054.3:p.Tyr382Cys
ENST00000369059.5:c.800A>G ENSP00000358055.1:p.Tyr267Cys
ENST00000369060.8:c.939+4717A>G ENSP00000358056.4:n.939+4717A>G
ENST00000369061.8:c.806A>G ENSP00000358057.4:p.Tyr269Cys
ENST00000457416.6:c.1145A>G ENSP00000410294.2:p.Tyr382Cys
ENST00000463870.5:n.351A>G
ENST00000478859.5:c.458A>G ENSP00000474011.1:p.Tyr153Cys
ENST00000604236.5:c.*189A>G ENSP00000474109.1:n.*189A>G
ENST00000613048.4:c.875A>G ENSP00000484154.1:p.Tyr292Cys
NM_000141.4:c.1142A>G NP_000132.3:p.Tyr381Cys
NM_001144913.1:c.1145A>G NP_001138385.1:p.Tyr382Cys
NM_001144914.1:c.806A>G NP_001138386.1:p.Tyr269Cys
NM_001144915.1:c.875A>G NP_001138387.1:p.Tyr292Cys
NM_001144916.1:c.797A>G NP_001138388.1:p.Tyr266Cys
NM_001144917.1:c.939+4717A>G NP_001138389.1:n.939+4717A>G
NM_001144918.1:c.797A>G NP_001138390.1:p.Tyr266Cys
NM_001144919.1:c.878A>G NP_001138391.1:p.Tyr293Cys
NM_022970.3:c.1145A>G NP_075259.4:p.Tyr382Cys
NM_023029.2:c.875A>G NP_075418.1:p.Tyr292Cys
NR_073009.1:n.1592A>G
XM_006717708.2:c.1202A>G XP_006717771.1:p.Tyr401Cys
XM_006717709.2:c.1199A>G XP_006717772.1:p.Tyr400Cys
XM_006717710.2:c.1202A>G XP_006717773.1:p.Tyr401Cys
XM_006717711.2:c.935A>G XP_006717774.1:p.Tyr312Cys
XM_006717712.2:c.857A>G XP_006717775.1:p.Tyr286Cys
XM_006717713.2:c.1199A>G XP_006717776.1:p.Tyr400Cys
XM_011539510.1:c.458A>G XP_011537812.1:p.Tyr153Cys
NM_001320654.1:c.458A>G NP_001307583.1:p.Tyr153Cys
NM_001320658.1:c.1142A>G NP_001307587.1:p.Tyr381Cys
XM_006717708.3:c.1202A>G XP_006717771.1:p.Tyr401Cys
XM_006717710.4:c.1202A>G XP_006717773.1:p.Tyr401Cys
XM_017015920.2:c.1202A>G XP_016871409.1:p.Tyr401Cys
XM_017015921.2:c.1199A>G XP_016871410.1:p.Tyr400Cys
XM_017015924.2:c.854A>G XP_016871413.1:p.Tyr285Cys
XM_017015925.2:c.854A>G XP_016871414.1:p.Tyr285Cys
XM_024447887.1:c.932A>G XP_024303655.1:p.Tyr311Cys
XM_024447888.1:c.935A>G XP_024303656.1:p.Tyr312Cys
XM_024447889.1:c.932A>G XP_024303657.1:p.Tyr311Cys
XM_024447890.1:c.935A>G XP_024303658.1:p.Tyr312Cys
XM_024447891.1:c.857A>G XP_024303659.1:p.Tyr286Cys
XM_024447892.1:c.-29A>G XP_024303660.1:n.-29A>G
NM_000141.5:c.1142A>G MANE Select NP_000132.3:p.Tyr381Cys
NM_001144917.2:c.939+4717A>G NP_001138389.1:n.939+4717A>G
NM_001144918.2:c.797A>G NP_001138390.1:p.Tyr266Cys
NM_001144919.2:c.878A>G NP_001138391.1:p.Tyr293Cys
NM_001320658.2:c.1142A>G NP_001307587.1:p.Tyr381Cys
NR_073009.2:n.1578A>G
NM_001144915.2:c.875A>G NP_001138387.1:p.Tyr292Cys
NM_001144916.2:c.797A>G NP_001138388.1:p.Tyr266Cys
NM_001320654.2:c.458A>G NP_001307583.1:p.Tyr153Cys
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