Canonical Allele Identifier: CA214324269
Gene: FGFR2 HGNC NCBI

Linked Data

dbSNP Id: rs561672600

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121594260C>T , CM000672.2:g.121594260C>T GRCh38
NC_000010.10:g.123353774C>T , CM000672.1:g.123353774C>T GRCh37
NC_000010.9:g.123343764C>T NCBI36
NG_012449.1:g.9199G>A
NG_012449.2:g.9199G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.-150-293G>A MANE Plus Clinical ENSP00000410294.2:n.-150-293G>A
ENST00000351936.11:c.-150-293G>A ENSP00000309878.10:n.-150-293G>A
ENST00000682550.1:c.-150-293G>A ENSP00000507633.1:n.-150-293G>A
ENST00000683035.1:c.-443G>A ENSP00000507074.1:n.-443G>A
ENST00000683211.1:c.-443G>A ENSP00000508257.1:n.-443G>A
ENST00000683250.1:c.-299G>A ENSP00000506847.1:n.-299G>A
ENST00000684153.1:c.-150-293G>A ENSP00000506937.1:n.-150-293G>A
ENST00000358487.10:c.-150-293G>A MANE Select ENSP00000351276.6:n.-150-293G>A
ENST00000636922.1:c.-150-293G>A ENSP00000490905.1:n.-150-293G>A
ENST00000336553.10:c.-150-293G>A ENSP00000337665.6:n.-150-293G>A
ENST00000356226.8:c.-150-293G>A ENSP00000348559.4:n.-150-293G>A
ENST00000357555.9:c.-150-293G>A ENSP00000350166.5:n.-150-293G>A
ENST00000358487.9:c.-150-293G>A ENSP00000351276.5:n.-150-293G>A
ENST00000359354.6:c.-150-293G>A ENSP00000352309.2:n.-150-293G>A
ENST00000360144.7:c.-150-293G>A ENSP00000353262.3:n.-150-293G>A
ENST00000369058.7:c.-150-293G>A ENSP00000358054.3:n.-150-293G>A
ENST00000369059.5:c.-150-293G>A ENSP00000358055.1:n.-150-293G>A
ENST00000369060.8:c.-150-293G>A ENSP00000358056.4:n.-150-293G>A
ENST00000457416.6:c.-150-293G>A ENSP00000410294.2:n.-150-293G>A
ENST00000490349.5:n.112-293G>A
ENST00000604236.5:c.-150-293G>A ENSP00000474109.1:n.-150-293G>A
ENST00000613048.4:c.-150-293G>A ENSP00000484154.1:n.-150-293G>A
NM_000141.4:c.-150-293G>A NP_000132.3:n.-150-293G>A
NM_001144915.1:c.-150-293G>A NP_001138387.1:n.-150-293G>A
NM_001144917.1:c.-150-293G>A NP_001138389.1:n.-150-293G>A
NM_001144918.1:c.-150-293G>A NP_001138390.1:n.-150-293G>A
NM_001144919.1:c.-150-293G>A NP_001138391.1:n.-150-293G>A
NM_022970.3:c.-150-293G>A NP_075259.4:n.-150-293G>A
NR_073009.1:n.498-293G>A
XM_006717708.2:c.-93-293G>A XP_006717771.1:n.-93-293G>A
XM_006717709.2:c.-93-293G>A XP_006717772.1:n.-93-293G>A
XM_006717710.2:c.-93-293G>A XP_006717773.1:n.-93-293G>A
XM_006717713.2:c.-93-293G>A XP_006717776.1:n.-93-293G>A
NM_001320658.1:c.-150-293G>A NP_001307587.1:n.-150-293G>A
XM_006717708.3:c.-93-293G>A XP_006717771.1:n.-93-293G>A
XM_006717710.4:c.-93-293G>A XP_006717773.1:n.-93-293G>A
XM_017015920.2:c.-93-293G>A XP_016871409.1:n.-93-293G>A
XM_017015921.2:c.-93-293G>A XP_016871410.1:n.-93-293G>A
XM_017015924.2:c.-93-293G>A XP_016871413.1:n.-93-293G>A
XM_017015925.2:c.-93-293G>A XP_016871414.1:n.-93-293G>A
XM_024447887.1:c.-93-293G>A XP_024303655.1:n.-93-293G>A
XM_024447888.1:c.-93-293G>A XP_024303656.1:n.-93-293G>A
XM_024447889.1:c.-93-293G>A XP_024303657.1:n.-93-293G>A
XM_024447890.1:c.-93-293G>A XP_024303658.1:n.-93-293G>A
XM_024447891.1:c.-93-293G>A XP_024303659.1:n.-93-293G>A
NM_000141.5:c.-150-293G>A MANE Select NP_000132.3:n.-150-293G>A
NM_001144917.2:c.-150-293G>A NP_001138389.1:n.-150-293G>A
NM_001144918.2:c.-150-293G>A NP_001138390.1:n.-150-293G>A
NM_001144919.2:c.-150-293G>A NP_001138391.1:n.-150-293G>A
NM_001320658.2:c.-150-293G>A NP_001307587.1:n.-150-293G>A
NR_073009.2:n.484-293G>A
NM_001144915.2:c.-150-293G>A NP_001138387.1:n.-150-293G>A