Canonical Allele Identifier: CA13253605
Gene: FGFR2 HGNC NCBI

Linked Data

dbSNP Id: rs11199993

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121531750G>C , CM000672.2:g.121531750G>C GRCh38
NC_000010.10:g.123291264G>C , CM000672.1:g.123291264G>C GRCh37
NC_000010.9:g.123281254G>C NCBI36
NG_012449.1:g.71709C>G
NG_012449.2:g.71709C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.748+6842C>G MANE Plus Clinical ENSP00000410294.2:n.748+6842C>G
ENST00000351936.11:c.748+6842C>G ENSP00000309878.10:n.748+6842C>G
ENST00000682400.1:n.403+6842C>G
ENST00000682550.1:c.403+6842C>G ENSP00000507633.1:n.403+6842C>G
ENST00000683211.1:c.748+6842C>G ENSP00000508257.1:n.748+6842C>G
ENST00000683250.1:c.403+6842C>G ENSP00000506847.1:n.403+6842C>G
ENST00000683418.1:n.3095+6842C>G
ENST00000683678.1:n.748+6842C>G
ENST00000684153.1:c.403+6842C>G ENSP00000506937.1:n.403+6842C>G
ENST00000358487.10:c.748+6842C>G MANE Select ENSP00000351276.6:n.748+6842C>G
ENST00000336553.10:c.481+6842C>G ENSP00000337665.6:n.481+6842C>G
ENST00000346997.6:c.748+6842C>G ENSP00000263451.5:n.748+6842C>G
ENST00000351936.10:c.748+6842C>G ENSP00000309878.9:n.748+6842C>G
ENST00000356226.8:c.403+6842C>G ENSP00000348559.4:n.403+6842C>G
ENST00000357555.9:c.481+6842C>G ENSP00000350166.5:n.481+6842C>G
ENST00000358487.9:c.748+6842C>G ENSP00000351276.5:n.748+6842C>G
ENST00000360144.7:c.481+6842C>G ENSP00000353262.3:n.481+6842C>G
ENST00000369056.5:c.748+6842C>G ENSP00000358052.1:n.748+6842C>G
ENST00000369058.7:c.748+6842C>G ENSP00000358054.3:n.748+6842C>G
ENST00000369059.5:c.403+6842C>G ENSP00000358055.1:n.403+6842C>G
ENST00000369060.8:c.748+6842C>G ENSP00000358056.4:n.748+6842C>G
ENST00000369061.8:c.748+6842C>G ENSP00000358057.4:n.748+6842C>G
ENST00000457416.6:c.748+6842C>G ENSP00000410294.2:n.748+6842C>G
ENST00000490349.5:n.1009+6842C>G
ENST00000604236.5:c.403+6842C>G ENSP00000474109.1:n.403+6842C>G
ENST00000613048.4:c.481+6842C>G ENSP00000484154.1:n.481+6842C>G
NM_000141.4:c.748+6842C>G NP_000132.3:n.748+6842C>G
NM_001144913.1:c.748+6842C>G NP_001138385.1:n.748+6842C>G
NM_001144914.1:c.748+6842C>G NP_001138386.1:n.748+6842C>G
NM_001144915.1:c.481+6842C>G NP_001138387.1:n.481+6842C>G
NM_001144916.1:c.403+6842C>G NP_001138388.1:n.403+6842C>G
NM_001144917.1:c.748+6842C>G NP_001138389.1:n.748+6842C>G
NM_001144918.1:c.403+6842C>G NP_001138390.1:n.403+6842C>G
NM_001144919.1:c.481+6842C>G NP_001138391.1:n.481+6842C>G
NM_022970.3:c.748+6842C>G NP_075259.4:n.748+6842C>G
NM_023029.2:c.481+6842C>G NP_075418.1:n.481+6842C>G
NR_073009.1:n.1050+6842C>G
XM_006717708.2:c.805+6842C>G XP_006717771.1:n.805+6842C>G
XM_006717709.2:c.805+6842C>G XP_006717772.1:n.805+6842C>G
XM_006717710.2:c.805+6842C>G XP_006717773.1:n.805+6842C>G
XM_006717711.2:c.538+6842C>G XP_006717774.1:n.538+6842C>G
XM_006717712.2:c.460+6842C>G XP_006717775.1:n.460+6842C>G
XM_006717713.2:c.805+6842C>G XP_006717776.1:n.805+6842C>G
NM_001320658.1:c.748+6842C>G NP_001307587.1:n.748+6842C>G
XM_006717708.3:c.805+6842C>G XP_006717771.1:n.805+6842C>G
XM_006717710.4:c.805+6842C>G XP_006717773.1:n.805+6842C>G
XM_017015920.2:c.805+6842C>G XP_016871409.1:n.805+6842C>G
XM_017015921.2:c.805+6842C>G XP_016871410.1:n.805+6842C>G
XM_017015924.2:c.460+6842C>G XP_016871413.1:n.460+6842C>G
XM_017015925.2:c.460+6842C>G XP_016871414.1:n.460+6842C>G
XM_024447887.1:c.538+6842C>G XP_024303655.1:n.538+6842C>G
XM_024447888.1:c.538+6842C>G XP_024303656.1:n.538+6842C>G
XM_024447889.1:c.538+6842C>G XP_024303657.1:n.538+6842C>G
XM_024447890.1:c.538+6842C>G XP_024303658.1:n.538+6842C>G
XM_024447891.1:c.460+6842C>G XP_024303659.1:n.460+6842C>G
NM_000141.5:c.748+6842C>G MANE Select NP_000132.3:n.748+6842C>G
NM_001144917.2:c.748+6842C>G NP_001138389.1:n.748+6842C>G
NM_001144918.2:c.403+6842C>G NP_001138390.1:n.403+6842C>G
NM_001144919.2:c.481+6842C>G NP_001138391.1:n.481+6842C>G
NM_001320658.2:c.748+6842C>G NP_001307587.1:n.748+6842C>G
NR_073009.2:n.1036+6842C>G
NM_001144915.2:c.481+6842C>G NP_001138387.1:n.481+6842C>G
NM_001144916.2:c.403+6842C>G NP_001138388.1:n.403+6842C>G